A clinical trial to compare the effect of laparoscopic tranverse abdominis plane block with non TAP block in pain management in patient undergoing laparoscopic ventral hernia repair.
Phase 4
- Conditions
- Health Condition 1: K43- Ventral hernia
- Registration Number
- CTRI/2024/04/066051
- Lead Sponsor
- DR C REVATHI
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Age above 18 yrs.
Who provide consent for the study.
All elective as well as emergency cases
All patients undergoing laparoscopic ventral hernia repair.
Exclusion Criteria
Pregnancy.
All patients undergoing open ventral hernia repair.
Patients requiring epidural analgesia.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To compare the need of analgesics on the day of operation between two groups TAP Block and non-TAP blockTimepoint: 1 year
- Secondary Outcome Measures
Name Time Method To determine effectiveness of TAP block in reduction of pain after surgery using VAS (visual analog scale) in intervention group. <br/ ><br> To determine the safety of laparoscopic guided TAP block in ventral hernia repair. <br/ ><br>Timepoint: 1 year