A study of pain following laparoscopic ventral hernia mesh repair.
Not Applicable
Completed
- Conditions
- Health Condition 1: K439- Ventral hernia without obstructionor gangrene
- Registration Number
- CTRI/2021/01/030678
- Lead Sponsor
- ady Hardinge Medical College
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 60
Inclusion Criteria
1 Patients having uncomplicated primary ventral or incisional hernial defects.
2 Midline defect with expected hernial width equal to or less than 10cm.
Exclusion Criteria
•Patients with multiple defects.
•Patient with associated groin hernia.
•Patients with recurrent ventral hernia following prior mesh repair.
•Patients who failed to understand NRS-11 scale.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method 1. Early post-operative painTimepoint: Post operative pain in first 24 hours
- Secondary Outcome Measures
Name Time Method Intraoperative surgeon workloadTimepoint: At base line;Operative timeTimepoint: At baseline