Comparison of 2 patches for pain relief in patients undergoing gall bladder surgery
Not Applicable
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2023/02/050001
- Lead Sponsor
- Ananta Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 80
Inclusion Criteria
1. Patients scheduled for elective laparoscopic cholecystectomy under general anaesthesia.
2. Patients aged between 18 – 60 years, of either sex.
3.Belonging to ASA (American Society of Anaesthesiology) class I, II
Exclusion Criteria
1.History of cardiovascular diseases e.g. Ischemic heart disease, conduction defects, etc.
2.History of compromised renal / hepatic / neuronal functions.
3.Uncontrolled hypertension and Diabetes
4.Pregnant or lactating women.
5.Drug allergy
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Time at which VAS more than 3 (DURATION OF ANALGESIA)Timepoint: VAS at 2 hour, 4 hour, 8 hour, 16 hour,20 hour, 24 hour post operatively
- Secondary Outcome Measures
Name Time Method Intraoperative Hemodynamics (Heart Rate, Blood Pressure, Spo2, Respiratory rate) <br/ ><br>Timepoint: Intraoperative Hemodynamics (Heart Rate, Blood Pressure, Spo2, Respiratory rate) <br/ ><br>;SEVERITY OF PAINTimepoint: VAS;Total number of rescue analgesics required in 24 hours postoperatively <br/ ><br>Timepoint: Total number of rescue analgesics required in 24 hours postoperatively