A comparative study of two different opioids in two different routes for postoperative analgesia in patients undergoing major abdominal surgeries
Phase 2
- Registration Number
- CTRI/2024/03/064238
- Lead Sponsor
- Bangalore medical college and research institute
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients with weight 40-80kgs.
Patients scheduled for open elective intraperitoneal abdominal surgeries under general anaesthesia
Patients giving informed written consent.
Patients belonging to ASA I, II.
Exclusion Criteria
1.Patients who refused to give informed written consent.
2.Patients with ASA physical status III or more.
3.Patients with known cardiac and pulmonary complications.
4.Patients with known allergy to opioids.
5.Patients with mental illness.
6.Pregnants and breastfeeding females.
7. Surgeries of duration > 3 hours.
8. Surgeries including surgical incision extended 5 cm above the umbilicus.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method visual analogue scale <br/ ><br>Timepoint: Post operative day 1 to day 3 <br/ ><br>
- Secondary Outcome Measures
Name Time Method ramsay sedation scale <br/ ><br>hemodynamic parameters <br/ ><br>adverse effectsTimepoint: post operative day 1 to 3