- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT02415543
SIL-TEP vs TEP for Inguinal Hernia Repair in Day Surgery
A Prospective, Randomized, Controlled Trial of Comparing Single Incisional Laparoscopic Total Extraperitoneal(SIL-TEP) Inguinal Hernia Repair With Traditional Laparoscopic Total Extraperitoneal(TEP) Inguinal Hernia Repair in Day Surgery
This study aim to compare the efficacy and safety of Single incisional Laparoscopic Total Extraperitoneal(SIL-TEP) Inguinal Hernia Repair and traditional Laparoscopic Total Extraperitoneal(TEP) Inguinal Hernia Repair in day surgery. This study also aim to improve the surgical-related technical details and the device design.
In addition, this study also evaluate the operability of SIL-TEP in term of a day surgery item and try to provide the basis for SIL-TEP day surgery guildline, so as to promote the SIL-TEP technology in the investigators country.
Study Overview
Status
Conditions
Intervention / Treatment
Detailed Description
This is a prospective, randomized,controlled trail. It compared Single Incisional Laparoscopic Total Extraperitonea(SIL-TEP) with traditional Laparoscopic Total Extraperitoneal(TEP) Inguinal Hernia Repair in condition of day surgery.
Laparoscopic hernia repair technique including two tyes, TEP and TAPP, which were recognized as mordern minimally invasive technique. Laparoscopic hernia repair were recommended by the Association of Surgeons of Great Britain and Ireland (ASGBI) and European Hernia Society Guideline (EHS) as the first choice for primary inguinal hernia. Compared with TAPP, TEP was performed much more frequently for its advantages of avoiding abdominal visceral injury.
Traditional TEP hernia repair involves 3-port insertions: one incision of 2cm in para-umbilical region for the camera and two smaller incisions of 5mm each in the midline for the surgical instruments. Some surgeons think the second and third ports could led to bowel and bladder injury. Early literatures showed that bowel injuries and bladder injuries were observed in TAPP or TEP hernia repair.
Since 2009, Cugura JF and Filipovic-Cugura J led their teams for a preliminary exploration of SIL-TEP. Later, several cases were reported about this surgical technique globally. Since then, a number of retrospective studies about the comparation of SIL-TEP and traditional TEP were carried. Yang GP et al found that SIL-TEP had a longer operation time than traditional TEP, but in terms of postoperative complications and incision aesthetics. Tu Wenbin et al thought that SIL-TEP was effective and also had advantages in postoperative pain, postoperative complications and time in hospital. Several other reports also had similiar opnions.
However, randomized controlled trial related to this suject is quite limited. Our study aim to compare the efficacy and safety of SIL-TEP and traditional TEP surgery with a RCT design and also aim to improve the surgical-related technical details and the device design. Our study also evaluate the operability of SIL-TEP in term of a day surgery item and try to provide the basis for SIL-TEP day surgery guildline, so as to promote the SIL-TEP technology in our country.
Study Type
Enrollment (Anticipated)
Phase
- Not Applicable
Contacts and Locations
Study Contact
- Name: TAO CHEN, MD
- Phone Number: 12157918664 +8613601779874
- Email: dr_chentao78@163.com
Study Locations
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Shanghai
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Shanghai, Shanghai, China, 200127
- Recruiting
- RenJi hospital
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Description
Inclusion Criteria:
- Diagnosed of primary unilateral inguinal hernia and age between 18 and 70 ;
- Good condition of family care and observation, understand and be willing to accept day surgery mode;
- Willing to participate in this study and signed an informed consent.
Exclusion Criteria:
- Diagnosed as femoral hernia, recurrent hernia, scrotal hernia, bilateral hernia and strangulated hernia;
- Patients with severe chronic diseases or cardiopulmonary dysfunction;
- American Society of Anesthesiologists (ASA) grade III and IV level;
- Obese patients ( BMI> 30 );
- Patients with a history of lower abdominal surgery;
- prefer to a centain surgical approach.
Study Plan
How is the study designed?
Design Details
- Primary Purpose: TREATMENT
- Allocation: RANDOMIZED
- Interventional Model: PARALLEL
- Masking: SINGLE
Arms and Interventions
Participant Group / Arm |
Intervention / Treatment |
---|---|
ACTIVE_COMPARATOR: GROUP A
Group A will undergo SIL-TEP inguinal hernia repair with a single port LESS (12 to 15 mm paraumbilical)
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perform the laparoscopic total extraperitoneal inguinal hernia repair using a single incision
Other Names:
|
ACTIVE_COMPARATOR: GROUP B
Group B will undergo laparoscopic TEP inguinal hernia repair with 3 ports (10 mm , and 2 ports of 5 mm )
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perform the multiport laparoscopic total extraperitoneal inguinal hernia repair
Other Names:
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
SIL-TEP Conversion to TEP / TAPP or open operation
Time Frame: during operation
|
This refers to whether any SIL-TEP procedure needs to be converted to TEP/TAPP or open procedure.
This is quite a normal process as a proportion of multiport procedures are converted to open procedures for safety reasons.
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during operation
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Secondary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
---|---|---|
Operating time
Time Frame: during operation
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This assess the time taken to perform the operation and is defined as time from initial skin incision to complete wound closure
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during operation
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interoperation complication
Time Frame: during operation
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Assessment of interoperation procedure of the incident of spermaduct、vessel and other organ damage
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during operation
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Pain score (Visual Analog Scale) at 12、24 hour and one week after surgery
Time Frame: 12、24hour and day 7 postoperation
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Assessment of post-operative pain according to the visual analog scale Pain score will be taken, and any painkiller consumption will be recorded
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12、24hour and day 7 postoperation
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Length of hospital stay
Time Frame: 1 day postoperation
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This assess how long patients stay in hospital and whether it is a day surgery or they need to extend time stay in hospital
|
1 day postoperation
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return to work or normal physical activities
Time Frame: 4 weeks postoperation
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Patients will be followed up and assesses how soon patients return to normal physical activities and work
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4 weeks postoperation
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Cosmetic scar score
Time Frame: 4 weeks
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Patients will be followed up and asked to assess satisfaction of their own scars 4 weeks postoperation
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4 weeks
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post-operative complications including urinary retention, wound infection, wound haematoma,seroma formation, chronic pain, testicular atrophy
Time Frame: 1 week, 4 weeks after postoperation
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Patients will be followed up and assessed at 1 week, 4 weeks after surgery to assess for any post-operative complications associated with hernia surgery as enumerated above
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1 week, 4 weeks after postoperation
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Recurrence of hernia
Time Frame: 4 weeks,3 mounths and 1 year postoperation
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Patients will be followed up and assessed at 4 weeks,3 mounths and one year after surgery to detect the presence of recurrence of hernia
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4 weeks,3 mounths and 1 year postoperation
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hospitalization costs
Time Frame: 1 day postopetation
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Hospitalization costs will be assessed after operation at discharge form the hospital
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1 day postopetation
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Collaborators and Investigators
Sponsor
Investigators
- Study Chair: JIAN WANG, MD, Director of Biliary and Pancreatic Surgery Department Renji Hospital, Shanghai Jiao Tong University, School of Medicine
Study record dates
Study Major Dates
Study Start
Primary Completion (ANTICIPATED)
Study Completion (ANTICIPATED)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (ESTIMATE)
Study Record Updates
Last Update Posted (ESTIMATE)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- RenJi Hospital
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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