Clinical Trial Details
— Status: Completed
Administrative data
| NCT number |
NCT01104727 |
| Other study ID # |
EAES-3 |
| Secondary ID |
|
| Status |
Completed |
| Phase |
Phase 4
|
| First received |
|
| Last updated |
|
| Start date |
April 2011 |
| Est. completion date |
July 2015 |
Study information
| Verified date |
July 2018 |
| Source |
European Association for Endoscopic Surgery |
| Contact |
n/a |
| Is FDA regulated |
No |
| Health authority |
|
| Study type |
Interventional
|
Clinical Trial Summary
The aim of this study is to compare results of the new surgical strategy to the traditional
4-ports technique for cholecystectomy in a randomized controlled trial (RCT). In particular
we are going to investigate the procedures in terms of overall morbidity, while taking into
considerations skin-incision's related morbidity, postoperative pain and cosmetic results
which are the hypothetical benefits of the new approach. Other parameters are supposed to be
unchanged, considering evidences from recent literature.
Surgical procedures:
4 ports cholecystectomy (4PC): a 12mmHg pneumoperitoeum is created either by a 10mm umbilical
Hasson's port or by a Verress needle followed by a 10mm umbilical port insertion; further one
10mm and two 5mm ports are placed according to the preferred technique.
Single Port Access cholecystectomy (SPC): the single-port device is inserted through the
umbilicus, by means of an adeguate incision, as the only access to the abdominal cavity. A
trans-abdominal suture in right hypochondrium is placed through the gallbladder wall of the
fundus to retract it.
Primary endpoint: overall morbidity rate (at 60 days from surgery)
Secondary endpoints:
1. skin-incision's related morbidity rate (at 60 days from surgery)
2. perioperative pain
3. cosmetic results
4. long-term morbidity (12 months)
5. intraoperative time
6. "conversion SPC to 4PC" rate
7. "conversion to laparotomy" rate
8. hospital stay
Description:
Duration of the project Patients will be recruited for this study from September 2010 until
September 2012 in all participating centers. All randomized patients will be followed up
(after recovery) with outpatient clinic appointments 30 and 60 days from surgery. A long-term
evaluation will be done 12 months after surgery. The last 3 months will be used for
photographic analysis of cosmetic results, statistical analysis and reporting of data.
Hypothesis /Aims SPA technique is a feasible approach to the peritoneal cavity. While
performing laparoscopic cholecystectomy the single umbilical access has an overall morbidity
comparable to multiport laparoscopy (equivalence study) while it entails a reduced
skin-incision's related morbidity rate, a reduced post-operative pain and allows a better
cosmetic result. Other considered parameters (operative time, conversion rate and hospital
stay) are supposed to be unchanged.
Background More recently Natural Orifice Translumenal Endoscopic Surgery (NOTES) has been
highlighted to the attention of lay literature and media, after first clinical reports.
Concept and feasibility had been tested in animal experiments since 20041, leading to the
creation of new scientific societies and committees with the declared aim to regulate
research activity, through sponsorships and registers, without reaching the goal completely.
After less than three years, the race for the first cholecystectomy under NOTES conditions in
a human being was having its course. Since then, many authors have reported various case
collections, while many others presented consistent research activity in vitro or in vivo,
but it looks evident that two different branches of research were being defined2 .
The first consists in what we would call Endoscopical Access Natural Orifice Surgery (EA-NOS)
which includes all procedures truly performed through natural orifices, having the goal to
design new platforms for surgery to be brought within the human body to recreate surgical
conditions under safety. The evident difficulties to obtain such an environment with
guaranteed ease of use, safety and efficacy, reduced to a mere research activity the interest
in this field, with few clinical applications described consisting of hybrid procedures, i.e.
procedures which were performed basically under laparoscopic conditions with the help of
flexible instruments inserted through natural orifices. In fact, a recent large metanalysis
of NOTES literature3 focusing on various surgical intra-abdominal procedures, all ascribable
to EA-NOS, concluded that no human studies were found satisfactory for the inclusion
criteria, for scarce disposable evidence, minor safety and efficacy compared to laparotomic
and laparoscopic alternatives. The recommendation that human procedures should first pass
through hybrid NOTES surgery, under strict guidelines, and in apposite controlled registers
was later supported, as known, by the revision of NOSCAR "white paper" 4 . In fact, it is out
of discussion that there is a need for a worldwide register, a standardization of the
nomenclature, safety data to be used by ethical committees in order to authorize human
trials, and implementation of the interface between medical societies, industry and
regulatory offices. In this field, on behalf of the EURONOTES Foundation, we have promoted an
european registry of NOTES procedures (www.euronotes.world.it) which preliminary results are
now awaited.
The cooling of enthusiasm related to EA-NOS procedures has naturally forced surgeons to
concentrate on techniques which could be more easily reproduced in clinical environments.
This brought the interest towards what we would call Surgical Access Natural Orifice Surgery
(SA-NOS)2 . In fact, an analysis of the literature would unveil that the vast majority of
human studies can be ascribed to SA-NOS. A wider vision of what can be considered a SA-NOS
approach, includes in this group not only transvaginal, thoroughly described in literature,
but also trans-umbilical surgery. Although both approaches have the advantage of not being
burdened by problems related to endoscopic defect's closure in terms of infection, safety,
consistent technological research and time-consumption, there is no discussion that
trans-umbilical techniques encountered more appreciation among surgeons. We have observed a
rapid clinical diffusion driven by a technology development supported by all the different
major surgical companies. Thus, it has to be said that single-port laparoscopic surgery is
nothing new. It was 1992 when Marco Pelosi first described a laparoscopic appendectomy using
a single umbilical puncture5 . Even multi-port single-incision trans-umbilical laparoscopic
cholecystectomy was first described by Giuseppe Navarra already in 19977 . Despite this,
interest towards single-port surgery grew-up only very recently. This might be on one side
explained with the better establishment of laparoscopic techniques and skills over the years,
but rises doubts about a possible industry driven interest.
There is no discussion that the technique has a number of drawbacks. The major one regards
the concept of "triangulation" to which laparoscopic surgeons have grown accustomed in terms
of both the instruments and scope, which is now lacking. Although this seems to be
overshadowed by the increasing acceptability of in-line viewing, it has to be said that
industries concentrate on developing and marketing a number of curved instrument with
different characteristics with the aim of restoring standard triangulation as under
laparoscopic environment. Nevertheless, personal experience gained by conducing a trial on a
virtual reality simulator designed for the purpose, demonstrated that only very experienced
surgeons performed surgical tasks with safety and effectiveness and requiring a short
learning curve, while for all other surgeons technique acquisition was challenging7 .
Still a number of different concerns arise. The fundamental hypotheses that were at the base
of single-port growing interest were that it could improve cosmesis, decrease post-operative
pain and therefore probably allow an earlier return to work with in any case a better
patient's satisfaction. None of these has been confirmed yet, if they will ever. It is also
clear that those who advocate patients' preference as the main reason for proposing
single-port techniques forget that patients' preference is deeply influenced by the
assumption that these arguments in favor of single-port surgery are correct, despite there is
no realistic certainty about it. Some of the major experts in the field of minimally invasive
surgery and active researchers in the field of NOTES share the same skeptical opinion about a
real benefit of single port techniques application. Dr Ratner for instance states in a recent
interview that "...it is not clear to me whether single port laparoscopy would be beneficial
compared to traditional laparoscopy"8 .
In any case we should never advocate for even slightly improved cosmetic value over safety,
the principal concern. This has implications in both the intraoperative and the postoperative
time. While it is recommended not to consider conversion to standard multi-trocars
laparoscopy a failure, it might be that, as it happened at the beginning of the diffusion of
laparoscopy, an increased number of complications will be observed. In fact, as often in
similar circumstances, only a minority of efforts has been dedicated to training programs and
very few simulators are available yet. Moreover, it has been advocated that a larger
peri-umbilical incision and consequent fascial defect would imply a higher rate of incisional
hernia. Although this is likely to happen, only time and data acquired will give us the
answer.
For these reasons robust studies to show that there is indeed a difference without a
significant compromise of safety should be awaited before a wide diffusion of these
techniques. In the proposed study cholecystectomy is chosen as a target as it represent the
typical and more diffuse indication for laparoscopy. Its morbidity rate related to skin
incisions occurs in a range of 1 to 5%9,10.
REFERENCES Kalloo AN, Singh VK, Jagannath SB, Niiyama H, Hill SL, Vaughn CA, Magee CA,
Kantsevoy SV (2004) Flexible transgastric peritoneoscopy: a novel approach to diagnostic and
therapeutic interventions in the peritoneal cavity. Gastrointest Endosc 60(1):114-117
Vettoretto N, Arezzo A. Human natural orifice translumenal endoscopic surgery: on the way to
two different philosophies? Surg Endosc. 2010 Feb;24(2):490-2.
Della Flora E, Wilson TG, Martin IJ, O'Rourke NA, Maddern GJ (2008) A review of natural
orifice translumenal endoscopic surgery (NOTES) for intra-abdominal surgery: experimental
models, techniques, and applicability to the clinical setting. Ann Surg 247(4):583-602 Hawes
RH (2008) Transition from laboratory to clinical practice in NOTES: role of NOSCAR.
Gastrointest Endosc Clin N Am 18(2):333-341 Pelosi MA, Pelosi MA 3rd. Laparoscopic
appendectomy using a single umbilical puncture (minilaparoscopy). J Reprod Med. 1992
Jul;37(7):588-94.
Navarra G, Pozza E, Occhionorelli S, Carcoforo P, Donini I. One-wound laparoscopic
cholecystectomy. Br J Surg. 1997 May;84(5):695 Rimonda R., Brown S., Tang B., Cuschieri A.
Ergonomic performance with crossed and uncrossed instruments in single port laparoscopic
surgery. Accepted for 12th SAGES (American Society of GastroEndoscopic Surgery) Congress,
Washington DC (USA), April 2010; under review on Annals of Surgery.
Rattner D. Single port surgery and NOTES: competition or transition?. Epublication:
WeBSurg.com, Nov 2007;7(11). URL: http://www.eats.fr/doi-vd02en2227rattner3e.htm
Access-related complications - an analysis of 6023 consecutive laparoscopic hernia repairs.
Minim Invasive Ther Allied Tecnol (2001) 1: 23-29 Hong T.H., You Y.K., Lee K.H.
Transumbilical single-port laparoscopic cholecysectomy. Surg Endosc (2008) DOI
10.1007/s00464-008-0252-y
Study Design Design: multi-centric randomized controlled trial (RCT)
Primary endpoint: Overall morbidity rate defined as any diagnosed morbidity related to
surgical technique within 60 days from surgery.
Primary outcome measure (for non-inferiority):
Morbidity, defined as the occurrence of any complication, directly or indirectly related to
surgery. Complications will be classified according to Dindo [Dindo D., Demartines N.,
Clavien PA. Classification of surgical complications: a new proposal with evaluation in a
cohort of 6336 patients and results of a survey. Ann Surg. 2004 Aug;240(2):205-13)]
Complications will be subdivided into procedural (during treatment) and delayed complications
(after ending the procedure), and further subdivided into major (requiring additional
surgery) and minor (requiring endoscopic or medical intervention) complications.
During admission patients will be monitored for complications. The following standardized
discharge criteria will be applied in all participating hospitals: normal intake of
nutrition; normal mobility; absence of fever (<38°C); and stable hemoglobin level during 1
day (<1 mmol/L).
In case of same day discharge from the hospital patients will be called by telephone 1 day
after the procedure whether adverse events have happened. Two weeks after the intervention, a
research nurse will contact the patient by telephone again and ask for occurred
complications.
The patient will undergo a direct check-up by means of a medical doctor at 30 and 60 days
after surgery, to conclude evaluation.
Secondary endpoints:
Skin-incision related morbidity defined as bleeding, infection, necrosis, skin retraction,
incisional hernia, suture dehiscence within 60 days from surgery.
Postoperative pain defined as a subjective evaluation of the same parameter using an
horizontal visual analogical scale daily for the first week and weekly till 60 days after
surgery. Patients will be administered Paracetamol IV 3 times a day for the first 24h, than
on demand. Tramadol will be administered when Paracetamol will not be judged sufficient for
pain control. On request, a single-dose of Ketorolac can be prescribed.
Cosmetic results defined as judgement of
- three independent surgeons: using a standardized methodology (patient on standing
position against a black background), two digital photographs (JPG format, 800x600
pixels resolution, 16x106 colours, 24 bit) will be taken preoperatively (for comparison)
and 60 days from surgery, one consisting of a close up of the umbilical area and a large
view including just the full abdomen. A Likert scale will be used independently by the
three surgeons to score the photographs from 1 to 5 (1= very poor, 2= poor, 3=
satisfactory, 4= good, 5= very good) in all cases. The mean value will be considered
objective evaluation of cosmetic outcome.
- the patient him/her self: the patient will be asked to score his/her subjective
perception of cosmetic outcome using the same Likert scale 60 days from surgery.
A following comparison of the two different measures will give an interesting proportion of
differences between subjective and objective perception.
Hospital stay: length (days) of hospital stay after surgery Intra-operative time: minutes
between skin incision and end of skin closure Conversion "Single-Port (SPC) to Multi-Ports
(4PC) Laparoscopy" rate: number of cases in which the surgeon preferred conversion from SPC
to 4PC for safely of technical reasons Conversion "to Open Surgery" rate: number of cases in
which the surgeon preferred conversion from SPC or 4PC to laparotomy for safely or technical
reasons.
Long term morbidity defined as any diagnosed morbidity related to surgical technique within 1
year from surgery.
Patient recruitment: Consecutive eligible patients will be recruited at the outpatient clinic
in the participating centres by the involved physician. All patients fulfilling the
above-mentioned criteria will be informed about the study by the physician. After consent is
given, central randomization will take place web-based and patients will be treated according
to the study protocol. Patients unable or refusing to provide informed consent will be
treated according to current clinical guidelines.
Randomization: patient data will be entered into a web-based database and a blind
randomization (into two experimental groups: a. traditional 4-Ports Cholecystectomy (4PC) vs.
b. Single-Port Cholecystectomy (SPC)) will be done by an unchangeable number-generating
software.
Blinding: Blinding of patients and physicians during treatment is unfeasible, since the two
treatment strategies are highly different and easily recognizable. Since a double-blinded
method is not possible in surgical experiments, this system guarantees the highest scientific
severity.
Study Population:
inclusion criteria: - age: 18-75
- BMI: <30 ASA: I-III absence of non-correctable coagulopathy (international normalized
ratio >1,5, or platelet count <90 × 109/l).
- diagnosis: cholelithiasis (gallstones < 2 cm in diameter) gallbladder dyskinesia
gallbladder polyps
exclusion criteria: - diagnosis: cholecystitis suspected presence of common duct stones
suspected presence of biliary cancer Previous abdominal surgery Previous umbilical surgery
Intervention techniques:
4-Ports Cholecystectomy (4PC): a 12mmHg pneumoperitoeum is created either by a 10mm umbelical
Hasson's port or by a Verress needle followed by a 10 mm umbelical port insertion; further
one 10mm and two 5mm ports are placed according to the preferred technique. A straight or
angulated laparoscope may be used. Laparoscopic graspers, monopolar hook, bipolar forceps,
scissors and 10mm clips-applier are used. A plastic bag system might be used for gall bladder
extraction if necessary. In both 10 and 12mm accesses, fascia is sutured with resorbable
sutures. Skin is secured by either metallic agraffes or interrupted sutures.
Single-Port Cholecystectomy (SPC): a 2.5cm long skin incision around the umbilicus is
performed. The subcutaneous tissue is dissected, the muscular fascia exposed and incised
along the middle line (linea alba) respecting the muscular tissue. Peritoneum is identified
and incised. The Single-Port device is inserted and anchored.
In order to retract the gallbladder a transcutaneous suture is placed in the right
hypocondrium with a straight needle and a monofilament thread which are passed through the
fundus and knotted outside the skin. The following steps reproduce the traditional
laparoscopic cholecystectomy. Each centre will be left free to use dedicated instruments and
which or traditional laparoscopic ones.
Complication/Intervention failure:
Conversion "single-port (SPC) to multi-ports (4PC) laparoscopy" is possible according to
surgeon's decision, while performing the surgical procedure. Since the patients' recruitment
is based on "intention to treat" the converted procedure will not be excluded from the study.
Conversion rate will be considered as a relevant result of the experiment.
Similarly, conversion "to open surgery" both from 4PC and SPC is possible according to
surgeon's decision, while performing the surgical procedure. Since the patients' recruitment
is based on "intention to treat", the converted procedure won't be excluded from the study.
Conversion rate will be considered as a relevant result of the experiment.
Sample size and Power calculation Assuming a baseline overall morbidity of 5% for both 4PC
and SPC group (average morbidity based on specific literature) and considering a level of
difference considered clinically significant of 0.05 (4.75 to 5.25%) for SPC to be
non-inferior, with a β-error of 0.2 and α-error of 0.05, 300 patients are needed per
randomization group.
600 patients in total allow to establish equivalence in terms of overall morbidity, with a
statistical power of 80%. If the hypothesis is confirmed, secondary endopoints will
eventually define benefits for the new surgical procedure in terms of reduced skin incision's
related morbidity, lower postoperative pain and better cosmetic results.
The sample size calculation has been obtained by R-software (R Project for Statistical
Computing, Lucent Technology, GNU General Public Licence) version 2.10.1, package epicalc,
routine sample-size.
Data analysis Intra and post-operative results will be inserted in the web-based database at
any time during the study by the recruiting surgeon. The photographic material will be
up-loaded into the computed database as well; all patients' personal data will be considered
strictly reserved in respect of privacy policy.
The Kolgoromow-test will be used to establish whether the results are parametric or not.
According to data feature, T-Test/Chi-Square or Wilcoxon rank test will be used where
appropriate. All analyses will be carried out primarily on an intention-to treat basis.
Impact on clinical practice and healthcare system SPA Surgery is an emergent frontier of
surgical innovation and represents an alternative to multi-ports standard laparoscopy. The
trans-umbilical technique allows to perform laparoscopy with the supposed benefit of reduced
invasiveness. In recent literature a large number of studies have aimed to demonstrate
feasibility and safety of the new method even if no randomized trial is still available for
definitive conclusions. Once feasibility and safety will be shown we will have to investigate
benefit for the patients. For these reasons we have chosen as primary endpoint overall
morbidity while in order to demonstrate the supposed benefit (patient's reduced discomfort
and better cosmetic outcome) and skin incision morbidity will be taken into consideration.
Since SPA surgical technique requires a consistent effort in terms of development of new
technology and surgeon's adaptation, we consider this definition of primary relevance. As a
matter of fact, a concrete introduction of SPA Surgery into daily practice is not possible
without a concrete advantage for patients. Except one single trial comparing only
postoperative pain (by Tsimoviannis et al. in G. Hatzikosta General Hospital, Ioannina
Greece), at present there are no similar studies posted on USA and European trials databanks.
For these reasons, we believe the MUSIC trial should produce precious information with
obvious recoils on clinical activity.
Track record of applicants including their experience in the field and any plot work carry
out The present MUSIC project is the result of a collaboration between the members of EAES
Technology Committee and the Board of the EAES. All applicants have big experience in the
field of new technologies in laparoscopic surgery. In particular, many of them have taken
part in development of new instruments and new techniques for trans-luminal endoscopic
surgery (NOTES). Since SPA surgery is considered part of this new concept for a
micro-invasive approach to the abdominal cavity, we consider their knowledge particularly
useful in the coordination of the trial. Considering the high interest on SPA-surgery
expressed in recent literature by the international surgical community, the Technology
Committee has developed a specific interest in this new branch of surgical innovation.
Mario Morino, Alberto Arezzo. Video Surgery through Single Port Access: an overview. Revista
Portuguesa de Cirurgia, in press Vettoretto N, Arezzo A. Human natural orifice translumenal
endoscopic surgery: on the way to two different philosophies? Surg Endosc. 2010
Feb;24(2):490-2. Epub 2009 Jul 2.
Arezzo A, Kratt T, Schurr MO, Morino M. Laparoscopic-assisted transgastric cholecystectomy
and secure endoscopic closure of the transgastric defect in a survival porcine model.
Endoscopy. 2009 Sep;41(9):767-72. Epub 2009 Aug 14.
Arezzo A, Morino M. Endoscopic closure of gastric access in perspective NOTES: an update on
techniques and technologies. Surg Endosc. 2010 Feb;24(2):298-303. Epub 2009 Jun 30.
Lirici MM, Arezzo A. Surgery without scars: the new frontier of minimally invasive surgery?
Controversies, concerns and expectations in advanced operative endoscopy. Minim Invasive Ther
Allied Technol. 2006;15(6):323-4.
Rimonda R., Brown S., Tang B., Cuschieri A. Ergonomic performance with crossed and uncrossed
instruments in single port laparoscopic surgery. Accepted for 12th SAGES (American Society of
GastroEndoscopic Surgery) Congress, Washington DC (USA), Aprile 2010; under review on Annals
of Surgery.
Neugebauer EA, Becker M, Buess GF, Cuschieri A, Dauben HP, Fingerhut A, Fuchs KH, Habermalz
B, Lantsberg L, Morino M, Reiter-Theil S, Soskuty G, Wayand W, Welsch T; On behalf of the
EAES. EAES recommendations on methodology of innovation management in endoscopic surgery.
Surg Endosc. 2010 Jan 7 Neugebauer EA, Morino M, Habermalz B. Surgical research or comic
opera? Let's give answers! Surg Endosc. 2008 Jun;22(6):1411-2.
Meining A, Kähler G, von Delius S, Buess G, Schneider A, Hochberger J, Wilhelm D, Kübler H,
Kranzfelder M, Bajbouj M, Fuchs KH, Gillen S, Feussner H.[Natural orifices transluminal
endoscopic surgery (NOTES) in Germany: summary of the working group reports of the "D-NOTES
meeting 2009"] Z Gastroenterol. 2009 Nov;47(11):1160-7 Fuchs KH, Breithaupt W. [Natural
orifice transluminal endoscopic surgery in future obesity treatment] Chirurg. 2008
Sep;79(9):837-42.
Sylla P, Rattner DW, Delgado S, Lacy AM. NOTES transanal rectal cancer resection using
transanal endoscopic microsurgery and laparoscopic assistance. Surg Endosc. 2010 Feb 26.
Lacy AM, Delgado S, Rojas OA, Ibarzabal A, Fernandez-Esparrach G, Taura P. Hybrid vaginal
MA-NOS sleeve gastrectomy: technical note on the procedure in a patient. Surg Endosc. 2009
May;23(5):1130-7. MA-NOS radical sigmoidectomy: report of a transvaginal resection in the
human. Surg Endosc. 2008 Jul;22(7):1717-23.
Project management structure
Once patients accept to be included in the MUSIC study, the randomization will be performed
in one of the two groups:
1. Treatment A: 4 Ports Cholecystectomy (4PC)
2. Treatment B: Single-Port Access Cholecystectomy (SPC) Randomization will take place by
connection to a dedicated web-site where initial data of the patient will be inserted
and the group assignment will be displayed, sent by e-mail to the centre logged in and
recruiting the patient, and stored in a dedicated database.
All the clinical informations related to the per-operative time and the follow-up as
described in the appendix will be stored through the same website and collected in a database
format. This will be accessible in an anonymous way, respecting the privacy of each patient,
at any time. Basic statistical analysis as well as more advanced data analysis such as
Wilcoxon tests and t-Student's test will be available online. Furthermore, the entire
database can be downloaded at anytime in xls format for more advanced data analysis.
This will allow to complete an interim analysis and report to the Ethical committee at any
time during the project. Proposed interval for analysis and reporting will be 3 months, if
not suggested differently.
All applicants will be in charge of collection of data and analysis of results.
Dissemination plan Dissemination of research results, training and exploitation will be
actively pursued. Results will be disseminated to the scientific community through
specialized media, as selected magazines, conferences, fairs, websites and medical society,
including clinicians considered final users and patients. Training activities will be carried
out based on the dissemination activities, the target of the courses is expected essentially
coming from the medical community.
The objective of the Dissemination Plan is to identify and organize the activities to be
performed in order to promote the exploitation of the project's results and the widest
dissemination of knowledge from the project.
MUSIC trial will establish an infrastructure for communications (and therefore dissemination)
by building a robust framework in which dialogue and interaction can take place. This applies
equally to internal and external communication. These will be used to disseminate information
about and solicit input into the Single-Port-Access Surgery project work. Contact can be
maintained and facilitated by electronic mailing lists, through Internal Lists within the
EAES members, and External Lists including stakeholders using several existing lists to
communicate to the wider community.
Moreover the MUSIC-working group develop a publications program which at minimum will
comprise:
targeted informational literature designed to raise awareness about Single-Port-Access
Surgery, and its activities instructional literature derived from experience across this
trial, including methodological guidelines and strategic guides to good clinical practice.
The MUSIC-working group will develop effective mechanisms for dissemination material
including the worldwide web, with a website which will include
- information about MUSIC study and its activities including contact details, background
information, working papers, events (seminars, workshops, conferences) etc.
- instructional materials as discussed above n(the web in this respect acts as a principal
means of publication):
- frequent news and updates to keep the community informed Finally printed publications
will be submitted to the EAES Official Journal, Surgical Endoscopy.
The MUSIC-working group will be promoting dissemination, advocacy and other events.
Conferences, workshops, seminars will be organized to:
raise awareness about activities, resources, results, etc.; act as training venues e.g. For
disseminating instructional material as required by a particular stakeholding community or
communities; act as for a for more public discussion of research, development, collections,
standards or other strategic and substantive issues of interest to SPA Surgery and the wider
community.
Long term sustainability of the work The program has the potential for long term
sustainability according to its underlying concept.
Since Single-Port surgery is a traditional laparoscopy-like technique, the cost of procedure
is expected to be similar. Other than different ports and instruments (already present on the
market), SPC and 4PC require the same laparoscopic equipment, largely available in every
operative room. From this point of view, the study doesn't imply any supplementary expense.
The follow up of both procedures is identical. It will consist in outpatient clinical
meetings and doesn't require expenses for new material and devices. Cost for complications
and hospital stay is supposed to be unchanged between the two experimental groups.
