Randomised Controlled Trial on Pre-peritoneal Drainage After Totally Extra-peritoneal Hernioplasty for Inguinal Hernia
- Conditions
- Hernia, Inguinal
- Interventions
- Procedure: preperitoneal suction drainage
- Registration Number
- NCT02762747
- Lead Sponsor
- The University of Hong Kong
- Brief Summary
This is a RCT on drain versus no drain after laparoscopic totally extra-peritoneal hernioplasty. We will assess the difference in seroma formation after surgery in 2 two groups by an independent assessor clinically and radiologist to document the size of seroma after surgery. Other secondary outcomes will be measured including post-operative pain, discomfort, analgesic used, patient satisfaction, recurrence of hernia, wound infection, etc.
- Detailed Description
Inguinal hernia is a common disease and causes significant morbidity if left untreated. With the advances of laparoscopic approach of extra-peritoneal hernioplasty, it significantly reduces the post-operative pain and lead to a better quality of life with higher acceptance to patients.However, similar to traditional Litchenstein approach, post operative seroma formation is still a common problem encountered after surgery. Numerous method has been described to reduce chance of seroma formation, however, none was proven to be effective except pre-peritoneal drainage. There are currently 2 large retrospective non-randomized cohort study to evaluate the effectiveness of preperitoneal drainage available for reference. We therefore study the feasibility and efficacy of preperitoneal drainage with large scale randomized trial.
Patient fulfill inclusion criteria and consent to surgery and study will be recruited. A standardized pre-peritoneal dissection and mesh placement will be adopted. Immediately before deflation of pre-peritoneal space, randomization will be performed by calling research assistant for study group using computer generated code. Drain will be placed for 23 hours after operation and ultrasonography will be performed immediately after removal of drain. USG will be repeated at post-operative 1 week, 1 month, 3 months, 6 months and 1 year after surgery. For non-drain group, a fake drain will be attach to the skin of the wound to achieve double blinding to patients and assessors. In addition to seroma, patient demographics and secondary outcome including post-operative pain score, discomfort, foreign body sensation, patient satisfaction, infection, recurrence, etc will be studied.
Recruitment & Eligibility
- Status
- UNKNOWN
- Sex
- All
- Target Recruitment
- 200
- Age above 18 and below 80
- Male or female patients
- Unilateral inguinal hernia
- First occurrence hernia
- Consent to laparoscopic hernioplasty for inguinal hernia
- Inguino-scrotal hernia
- Recurrent inguinal hernia
- Incarcerated hernia
- Bilateral inguinal hernia
- Bleeding tendency
- On anti-platelet agent or anti-coagulant
- Co-morbidies
- Decline or not consent to surgery
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- SINGLE_GROUP
- Arm && Interventions
Group Intervention Description Drain preperitoneal suction drainage preperitoneal suction drainage after laparoscopic totally extra-peritoneal hernioplasty for inguinal hernia
- Primary Outcome Measures
Name Time Method Seroma formation after TEP hernioplasty post-operative 1 year Seroma will be assessed clinically by independent assessor who is blind to the group assigned and also by qualified radiologist who will perform USG to measure the exact size of seroma formation after TEP
- Secondary Outcome Measures
Name Time Method Post-operative pain after TEP hernioplasty post-operative day 1 to day 7, 1 month, 3 month, 6 month, 1 year Post-operative pain after TEP hernioplasty will be assessed by self-evaluated VAS questionnaire during initial 7 days after operation. Then will be asked by independent assessor upon follow-up
Analgesic used after after TEP hernioplasty post-operative day 1 to day 7, 1 month, 3 month, 6 month, 1 year Number of analgesic used after after TEP hernioplasty will be assessed by self-evaluated questionnaire during initial 7 days after operation. Then will be asked by independent assessor upon follow-up
Hernia recurrence after TEP hernioplasty post-operative 1 month, 3 month, 6 month, 1 year Hernia recurrence after TEP hernioplasty will be assessed by independent assessor upon follow-up
Chronic discomfort after TEP hernioplasty post-operative 1 month, 3 month, 6 month, 1 year Chronic discomfort after TEP hernioplasty will be asked by independent assessor upon follow-up
Patient satisfaction after TEP hernioplasty post-operative 1 month, 3 month, 6 month, 1 year Patient satisfaction after TEP hernioplasty will be asked by independent assessor upon follow-up
Trial Locations
- Locations (1)
Department of Surgery, The University of Hong Kong - Shenzhen Hospital
🇨🇳Shenzhen, China