Comparing the post operative pain using two different methods of intravenous analgesia (one method by continuous intravenous infusion via dosifuser and other with patient controlled intravenous analgesia via CADD pump) in laparoscopic IPOM surgeries
Phase 3
- Conditions
- Health Condition 1: K439- Ventral hernia without obstructionor gangrene
- Registration Number
- CTRI/2024/04/065490
- Lead Sponsor
- K. Alwin Mesak
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1.Patients undergoing laparoscopic IPOM surgeries for midline ventral hernia
2.ASA I & II
3.Age between 18 and 70years
4.Normal renal function (serum creatinine less than or equal to 1.4mg/dl)
Exclusion Criteria
Not provided
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method