Inguinal Hernia Clinical Trial
— SILSTEPOfficial title:
Prospective Randomized Single Blind Controlled Study Comparing Single and Multiport Laparoscopic Total Extraperitoneal Inguinal Hernia Repair
Since laparoscopic inguinal hernia was introduced in 1990, it has now become the most
commonly performed hernia repair in NSW. Traditionally this is done with 3 small incisions:
a 2 cm incision under the navel for insertion of the camera and two 1 cm incisions below the
navel for insertion of trocars into which dissecting instruments are inserted to perform the
repair. Although this method has been shown to be relatively safe and efficient there are
reports of bowel and vascular injuries from the insertion of the smaller trocars which are
usually sharp. These can cause serious injuries.
Since 2009, a newer method of performing the key hole repair has been developed. This
involves placing a special single port under the navel via a 2-2.5cm incision and into which
3 blunt trocars are inserted. This negates the risks of injuries from sharp trocars. In
addition the fact that only a single incision is used this could potentially result in less
pain, reduced incidence of wound complications including infection and improved cosmetic
results.
However these potential advantages have not been proven in rigorous clinical studies as the
single port technique is still relatively new. It is hoped that this study will prove that
the single port technique is at least as effective and efficient as the conventional
technique in the cure of hernias and may have additional benefits as enumerated above.
Neither you nor your surgeon will know which procedure (three port or single port hernia
repair) until you are already asleep in the operating room and a random number selecting
process will automatically assign you to one procedure or the other. Sometimes it is not
possible to perform the single port safely in which case your procedure will be converted to
a three ports procedure.
All patients having surgical treatment of groin hernia at Holroyd Private Hospital are
subject to very careful assessment and study. All patients are requested to report
immediately if there are any problems. Any problems would normally be reported to your
treating surgeon who has primary responsibility for your care. Problems can be reported
directly to Holroyd Private Hospital. Any information in your medical records is subject to
stringent confidentiality requirements. The hospital is bound by the Australian Privacy
Council Charter as regards confidentiality and privacy.
Status | Completed |
Enrollment | 100 |
Est. completion date | March 2013 |
Est. primary completion date | January 2013 |
Accepts healthy volunteers | No |
Gender | Both |
Age group | 16 Years to 86 Years |
Eligibility |
Inclusion Criteria: - all referred patients with inguinal hernias Exclusion Criteria: - workers Compensation cases - previous extraperitoneal intervention - unfit for a general anaesthetic - strangulated hernias - present of or previous ventral hernia repair extending 5 cm below umbilicus |
Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Single Blind (Subject), Primary Purpose: Treatment
Country | Name | City | State |
---|---|---|---|
Australia | Holroyd Private Hospital | Guildford | New South Wales |
Lead Sponsor | Collaborator |
---|---|
The Sydney Hernia Specialists Clinic | University of Sydney |
Australia,
Tran H. Robotic single-port hernia surgery. JSLS. 2011 Jul-Sep;15(3):309-14. doi: 10.4293/108680811X13125733356198. — View Citation
Tran H. Safety and efficacy of single incision laparoscopic surgery for total extraperitoneal inguinal hernia repair. JSLS. 2011 Jan-Mar;15(1):47-52. doi: 10.4293/108680811X13022985131174. — View Citation
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Conversion to multiport or open operation | This refers to whether any single port procedure needs to be converted to multiports or open procedure. This is quite a normal process as a proportion of multiport procedures are converted to open procedures for safety reasons. | during operation | Yes |
Secondary | Operating time | This assess the time taken to perform the operation and is defined as time from initial skin incision to complete wound closure | during operation | Yes |
Secondary | Length of hospital stay | This assess how long patient stays in hospital whether it is a day procedure or whether they need to stay in hospital overnight or longer | day procedure or overnight stay | Yes |
Secondary | Pre and post operative pain scores | This utilizes the visual analogue pain score 0-10 and the patients are assessed preoperatively, day 1 and day 7 after surgery | preop, day one and day 7 postop | Yes |
Secondary | Analgesic requirements | This assesses how many painkiller tablets (Dextropropoxyphene) patients ingest in the first week after operation | one week | Yes |
Secondary | return to work or normal physical activities | This assesses how soon patients return to work or normal physical activities | 6 weeks | Yes |
Secondary | Quality of life health scores | SF36 forms are completed before operation, 6 weeks and 1 year after operation | preop, 6 weeks and 1 year postop | Yes |
Secondary | Cosmetic scar score | patients will be asked to assess satisfaction of their own scars 6 weeks after surgery | 6 weeks | Yes |
Secondary | Recurrence of hernia | Patients will be assessed at 1 week, 6 weeks and one year to detect presence of recurrence of hernia | 1 year | Yes |
Secondary | post-operative complications including urinary retention, wound infection, seroma formation, chronic pain, testicular atrophy | Patients will be seen at 1 week, 6 weeks to assess for any peri-operative complications associated with hernia surgery as enumerated above | 6 weeks | Yes |
Status | Clinical Trial | Phase | |
---|---|---|---|
Completed |
NCT03023462 -
Efficacy of an Anterior Quadratus Lumborum Block vs. a TAP-block for Inguinal Hernia Repair
|
N/A | |
Completed |
NCT04272320 -
The Efficacy of Transversalis Fascia Plane Block in Pediatric Inguinal Hernia Repair
|
N/A | |
Recruiting |
NCT03904888 -
Conventional Versus Robot Assisted Laparoscopic Inguinal Hernia Repair
|
N/A | |
Recruiting |
NCT03856710 -
Self Fixating Versus Stapled Mesh for Laparoscopic Inguinal Hernia Repair
|
N/A | |
Completed |
NCT02240550 -
A Comparative Clinical Study to Evaluate the Effectiveness of ProFlor vs. Lichtenstein for Inguinal Hernia Repair
|
N/A | |
Completed |
NCT01943760 -
Tamadol Wound Infiltration in Children Under Inguinal Hernioplasty
|
Phase 4 | |
Completed |
NCT01679353 -
Comparison of Analgesic Effect of Magnesium Added to Ropivacaine and Ropivacaine Alone in Caudal Analgesia on Postoperative Pain Control in Pediatric Patients Undergoing Inguinal Hernia Repair
|
N/A | |
Recruiting |
NCT01450345 -
Efficacy of Pre-operative Oral Pregabalin in Ambulatory Inguinal Hernia Repair for Post Operative Pain
|
Phase 3 | |
Active, not recruiting |
NCT00968773 -
Rebound Hernia Repair Device Mesh Trial
|
Phase 4 | |
Completed |
NCT01000116 -
Fibrin Glue Versus Tacked Fixation in Groin Hernia Repair (TAPP)
|
N/A | |
Completed |
NCT01117337 -
Comparing Non-fixation of Mesh to Mesh Fixation in Laparoscopic Inguinal Hernia Repair
|
Phase 4 | |
Terminated |
NCT00226161 -
Chronic Pain After Inguinal Herniorrhaphy
|
N/A | |
Completed |
NCT05837013 -
Open and Laparoscopic Total Extraperitoneal Repair Under Spinal Anesthesia Versus General Anesthesia
|
N/A | |
Recruiting |
NCT05058378 -
Correlation Between Spinal Anesthesia and Perfusion Index
|
||
Completed |
NCT01637818 -
Long-term Follow-up of Lichtenstein's Operation Versus Mesh Plug Repair
|
N/A | |
Recruiting |
NCT05879770 -
Is the Use of Prolene as Sufficient as the Use of Wire in Shouldice Surgery to Keep the Recurrence Rate Low After One Year?
|
||
Completed |
NCT05159232 -
Length of Hospital Stay in Laparoscopic Transabdominal Preperitoneal Vs. Open Mesh Repair in Inguinal Hernia: A Randomised Controlled Trial
|
N/A | |
Completed |
NCT05107986 -
Laparoscopy in Complicated Groin Hernia
|
||
Active, not recruiting |
NCT04328597 -
Portuguese Inguinal Hernia Cohort (PINE) Study
|
||
Completed |
NCT04033055 -
Antalgic Efficacy of CycloMeshâ„¢ Soaked in Ropivacaine Hydrochloride in Uncomplicated Inguinal Hernia.
|
N/A |