Pain Clinical Trial
Official title:
The Effect of Transvaginal vs. Conventional Laparoscopic Cholecystectomy on the Postoperative Course
Uncomplicated laparoscopic cholecystectomy will in most patients result in moderate to
severe pain until the first postoperative day. This will subside during the second and third
postoperative day [1]. A feeling of low general well-being will also be present until the
first postoperative day and subside during the next couple of days [2].
To achieve faster recovery after laparoscopic interventions it has been shown that a
reduction in the size of laparoscopic ports and thereby incisions can reduce postoperative
pain [3,4].
A new minimal invasive surgical technique is based on the principle of completely
eliminating the use of ports through the abdominal wall. This new technique is called
Natural Orifice Transluminal Endoscopic Surgery (NOTES) and is defined by acquiring minimal
invasive access to the abdominal cavity through the body's natural openings like the mouth
and stomach, anus, urethra and vagina. With the NOTES technique one can completely avoid
incisions in the abdominal wall and thereby reduce the surgical trauma. The benefits of this
technique is a reduction of postoperative pain, elimination of incisional hernias,
prevention of wound infections, reduction of peritoneal adherence formation, achieving a
faster recovery and a better cosmetic result [7,8].
The most documented and well-described way for gaining NOTES access to the abdominal cavity
is through the vagina, transvaginal (TV). TV NOTES has mainly been used for cholecystectomy
because of the direct line of vision to the upper abdomen and gallbladder that is achieved
through this opening.
Compilation of results show that TV NOTES cholecystectomy can be implemented with low
complication rates [20-22]. One retrospective case-control and one prospective observational
study report less postoperative pain, reduced consumption of analgesics and faster recovery
for TV NOTES compared to conventional laparoscopic cholecystectomy [23,24]. To date there
are no systematic prospective randomized data on whether or not TV NOTES cholecystectomy
leads to a better surgical outcome.
In the present study the postoperative course after TV NOTES cholecystectomy will be
compared to laparoscopic cholecystectomy in a prospective randomized and blinded trial. The
outcome of the randomization between the two surgical techniques will be blinded to patient
and the nurse staff for the first 72 hours after the operation. The primary outcome
parameter will be postoperative pain score during the first 24 hours. Secondary outcome
parameters are postoperative pain score for the first 72 hours, fatigue, well-being, nausea,
consumption of analgesics, complications, cosmetic result and sexual function.
The hypothesis being that TV NOTES cholecystectomy gives less postoperative pain, fatigue
and nausea, a reduction in analgesics and a better cosmetic result and general well-being
than conventional 4 port laparoscopic cholecystectomy.
BACKGROUND:
Uncomplicated laparoscopic cholecystectomy will in most patients result in moderate to
severe pain up until the first postoperative day. This will subside during the second and
third postoperative day [1]. A feeling of low general well-being will also be present up
until the first postoperative day and subside during the next couple of days [2].
To achieve faster recovery after laparoscopic interventions it has been shown that a
reduction in the size of laparoscopic ports and thereby incisions can reduce postoperative
pain [3,4]. Whether a further reduction of postoperative pain can be achieved by limiting
the number of laparoscopic ports through the abdominal wall to a single one with Single
Incision Laparoscopic Surgery (SILS) remains to be determined [5,6].
A new minimal invasive surgical technique is based on the principle of completely
eliminating the use of ports through the abdominal wall. This new technique is called
Natural Orifice Transluminal Endoscopic Surgery (NOTES) and is defined by acquiring minimal
invasive access to the abdominal cavity through the body's natural openings like the mouth
and stomach, anus, urethra and vagina. With the NOTES technique one can completely avoid
incisions in the abdominal wall and thereby further reduce the surgical trauma. The benefits
of this technique is a reduction of postoperative pain, elimination of incisional hernias,
prevention of wound infections, reduction of peritoneal adherence formation, achieving a
faster recovery and a better cosmetic result [7,8].
The most documented and well-described way for gaining NOTES access to the abdominal cavity
is through the vagina, transvaginal (TV). There are several reasons for this. First of all
the technique for gaining TV access to the abdominal cavity is already being used in
gynaecology, where culdoscopy was first described in the literature nearly 100 years ago
[9]. A diagnostic procedure for infertility that can be used in an outpatient setting
[10-12]. Similarly, transvaginal ports have been used in gynaecology as a substitute for
abdominal ports [13,14]. Thus there is already a well proven and established technique for
obtaining transvaginal access to the abdominal cavity. Secondly it is easy to ensure a
secure surgical closure of the point of entry under direct visualization with basic suturing
instruments. And lastly the risk of contamination and infection is minimal when performing
TV procedures [15].
TV NOTES has mainly been used for cholecystectomy because of the direct line of vision to
the upper abdomen including the liver and gallbladder that is achieved through this body
opening. For the same reason it is possible to use the same surgical dissection technique
and rigid instruments that is used when performing conventional laparoscopic or SILS
cholecystectomies.
Questionnaire surveys have shown that there is a general interest for TV NOTES in the
public, where between 33-68 % of women surveyed preferred TV NOTES to conventional
laparoscopy [16-18].
In a German national database called German NOTES Registry (GNR) more than 900 transvaginal
procedures have been registered. Compilation of results from the GNR and other human series
and multicenter trials have shown that TV NOTES cholecystectomy can be implemented with low
complication rates [19-21]. One retrospective case-control and one prospective observational
study report less postoperative pain, reduced consumption of analgesics and faster recovery
for TV NOTES cholecystectomy compared to conventional laparoscopic cholecystectomy [22,23].
To date there are no systematic prospective randomized data on whether or not TV NOTES
cholecystectomy leads to a better surgical outcome in regards to pain, well-being etc. than
conventional laparoscopic cholecystectomy.
STUDY AIM:
The aim of the study is in a prospective randomized blinded design to compare the
postoperative course and outcome of TV NOTES and conventional laparoscopic cholecystectomy.
HYPOTHESIS:
TV NOTES cholecystectomy gives less postoperative pain, fatigue and nausea, reduces
analgesic consumption and gives a better cosmetic result and well-being than conventional 4
port laparoscopic cholecystectomy.
TRIAL PARTICIPANTS:
Trial participants will be recruited among women between 40-75 years referred to
laparoscopic cholecystectomy due to symptomatic gallstones or gallstone induced mild
pancreatitis and ultrasonography confirmed gallstones.
METHOD:
Statistics:
The primary outcome measure "cumulated pain score during mobilisation for the first 72
postoperative hours" has been used for power calculation. In a previous study the mean for
this parameter measured on the visual analogue scale (VAS) for laparoscopic cholecystectomy
have been found to be 143 mm (standard deviation 95,7 mm) [2]. Since the pain sensation
after laparoscopic cholecystectomy is somatic in origin a MERIDIF of 60% (86mm) have been
chosen. Type I and type II errors have been set to 0,05 and 0,20 respectively. This gives a
total number of 42 participants with 21 in allocated to either group. To account for
potential dropouts and the lack of Gaussian distribution for VAS data there will be included
a total of 60 participants with 30 allocated to either group.
Non-parametric statistics with Fisher´s exact test, Mann-Whitney test and confidence
intervals will be used where appropriate. P < 0,05 will be considered statistical
significant. Drop-outs will be replaced by new participants until a minimum of 30
participants have been included in either group. Data will be analysed with intention-to
treat and per-protocol and the results of both methods will be published.
In the TV NOTES group the use of at least one 5mm trans-abdominal port will be considered as
a conversion to conventional laparoscopic surgery and will analysed as such. The use of one
Minilap instrument in the TV NOTES group will not be considered as a conversion to
laparoscopy and the participant will remain in the TV NOTES group for both the
intention-to-treat and the per-protocol analyses. Participants with severe intra-operative
complications will be excluded from the analyses but will be described separately in the
publication.
Randomization:
Participants will be randomized to either TV NOTES cholecystectomy or conventional
laparoscopic 4 port cholecystectomy. The randomization will be performed shortly before the
operation commences using the envelope method by the operating surgeon. All procedures will
be performed by the same surgeon at University Hospital Gentofte/Herlev, Copenhagen,
Denmark.
Blinding:
The trial is patient and observer blinded to the allocation of the randomization for the
first 72 hours of the postoperative course. Operating room staff and surgeons will not
participate in any way in the follow-up for the first 72 postoperative hours.
Participants in both groups will receive the same surgical dressing on the abdomen after the
procedure. Both groups will thus be bandaged as if after a conventional 4 port laparoscopic
cholecystectomy with a total of 4 dressing strips. In the TV NOTES group these dressings
will be stained red to simulate light seepage from the "wound". These dressings are
obligatory for the first 72 postoperative hours.
Informed consent:
The participants will receive oral and written information about the trial, its purpose and
potential benefits and risks. Participants will be informed that it is voluntary to
participate at that they at any time can withdraw their consent to participate in the trial
without it having any implications on present or future treatment. Written consent to
participate in the trial will be obtained before enrolment. National guidelines from the
Danish National Committee on Biomedical Research Ethics concerning informed content will be
followed.
Any information or medical considerations concerning the individual participant obtained as
part of the trial will be accessible to the participant.
ETHICAL CONSIDERATIONS:
TV NOTES cholecystectomy are based on well-established surgical techniques such as
laparoscopy/SILS and culdotomy. Complication types and rates for TV NOTES cholecystectomy
are well described in the literature and are comparable to that of conventional laparoscopic
cholecystectomy. Considering the advantages and theoretical benefits this new technique has
to offer combined with the preliminary retrospective and non-randomized results we find it
ethical to conduct a randomized controlled blinded trial where the benefits of TV NOTES
cholecystectomy outweighs the potential risks involved.
LAW AND APPROVAL:
The trial will be carried out according to the Helsinki Declaration II and under the Acts of
the Danish Council of Ethics and information concerning the participants will be protected
in accordance to the regulations set by the Danish Protection Agency. The trial will be
approved by the Danish National Committee on Biomedical Research Ethics, the Danish
Protection Agency and ClinicalTrials.gov before it is commenced.
FUNDING:
This trial is part of a PhD-study initiated by the trial investigators. Salaries are funded
through grants obtained from the University of Copenhagen, Herlev Hospital Research Council,
Capitol Region of Denmark Research Foundation for Health Research and private foundations.
Operating costs are founded through grants from private foundations. There are no commercial
interests in or financial support for the project.
PUBLICATION:
After the trial have been completed both positive and negative result will be published in
an internationally recognised scientific journal. The primary investigator in this trial
will be first-author and the co-investigators co-authors according to the Vancouver Group
criteria (www.icmje.org).
;
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment
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