Laparscopic Hernioplasty in Recurrent Inguinal Hernia
- Conditions
- Recurrent Inguinal Hernia
- Interventions
- Procedure: Total extraperitoneal (TEP) hernioplasty using polyprolene meshProcedure: Transabdominal preperitoneal (TAPP) using polyprolene mesh
- Registration Number
- NCT06050538
- Lead Sponsor
- Mansoura University
- Brief Summary
The purpose of this study was to compare between laparoscopic transabdominal preperitoneal (TAPP) and totally extraperitoneal (TEP) repair of inguinal hernia in recurrent inguinal hernia.
- Detailed Description
The primary objective in this study was to compare postoperative pain between the TAPP group and the TEP group. The secondary objective was to compare operative time, intraoperative complications (bleeding, bowel injury, vascular injury), postoperative complications (hematoma, seroma, wound infection), length of hospital stay and recurrence rate with possible risk factors which include gender, age, BMI ,cord lipomas and location of the hernia.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 44
- Patients diagnosed with unilateral or bilateral recurrent inguinal hernias.
- Patients between 18 and 70 years old
- Fit for anesthesia.
- Agree to participate in the study
- Both genders were included.
- Unfitness for general anesthesia and operation.
- Age < 18 years or >70 years.
- Complicated hernias (acute irreducible, obstruction or strangulation).
- The presence of mental or psychological disorders.
- Refusal to participate in the study.
Study & Design
- Study Type
- INTERVENTIONAL
- Study Design
- PARALLEL
- Arm && Interventions
Group Intervention Description Total extraperitoneal (TEP) approach Total extraperitoneal (TEP) hernioplasty using polyprolene mesh patients with recurrent inguinal hernia who had Total extraperitoneal (TEP) approach Transabdominal preperitoneal (TAPP) Transabdominal preperitoneal (TAPP) using polyprolene mesh patients with recurrent inguinal hernia who had Transabdominal preperitoneal (TAPP) approach
- Primary Outcome Measures
Name Time Method Postoperative pain 6 months by use of visual analog scale (VAS) where (0) refereed to no pain and (10) refereed to the severest pain.
- Secondary Outcome Measures
Name Time Method operative time 6 months operative time by minutes was reported to get mean and standard deviation
complications 6 months complications will be described as number and percentages in each group
Trial Locations
- Locations (1)
Mansoura University Hospitl
🇪🇬Mansoura, Egypt