Comparing non-fixation of mesh to mesh fixation in laparoscopic inguinal hernia repair
Not Applicable
Completed
- Registration Number
- CTRI/2009/091/000020
- Lead Sponsor
- Self
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 100
Inclusion Criteria
All reducible inguinal hernias will be included in the study.
Exclusion Criteria
Irreducible hernia after anesthesia, obstructed and strangulated hernias, pediatric hernias and patients with associated other hernias like ventral hernias will be excluded from the study. Patients unfit for spinal anesthesia will also be excluded from the study.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Recurrence rateTimepoint: 6 months
- Secondary Outcome Measures
Name Time Method Days to resume workTimepoint: 1 week;PainTimepoint: Post operative-6 hours, 24 hours, 1 week