EVALUATION OF POST OPERATIVE PAIN AFTER GIVING PRE-EMPTIVE ANALGESIA WITH PARACETAMOL IN OPEN INGUINAL HERNIA MESH REPAIR.
Phase 4
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/04/065619
- Lead Sponsor
- Dr Nandini Jain
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
age 18 and above
unilateral Lichtenstein inguinal hernia mesh repair under spinal anaesthesia
a?a grade 1 and 2
informed consent
Exclusion Criteria
hypersensitivity to paracetamol
different procedure for inguinal hernia
epidural anaesthesia
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method VAS pain score decreases significantly <br/ ><br>Need for rescue analgesia reducedTimepoint: 6hrs, 12hrs, 24hrs, 36hrs, 48hrs, 72hrs
- Secondary Outcome Measures
Name Time Method REDUCTION IN USE OF RESCUE ANALGESIA LIKE DICLOFENAC OR TRAMADOLTimepoint: 6hrs, 12hrs, 24hrs, 36hrs, 48hrs,72hrs