Comparison Of Intravenous Paracetamol, Intravenous Diclofenac And Their Combination For Perioperative Analgesia In Patients Undergoing Laparoscopic Cholecystectomy
Phase 1
- Conditions
- Health Condition 1: K87- Disorders of gallbladder, biliarytract and pancreas in diseases classified elsewhere
- Registration Number
- CTRI/2019/01/017097
- Lead Sponsor
- Department Of Anaesthesia Vardhman Mahavir Medical college And Safdarjung Hospital New Delhi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. Adult patients scheduled to undergo elective laparoscopic cholecystectomy under general anaesthesia
2.Age 18-65 years,either gender.
3.Patients fulfilling American Society of Anesthesiologists physical status I or II .
4.Weight 45-75 kgs.
5.BMI less than or equal to 35
Exclusion Criteria
1.Patient with known allergy to PCM/diclofenac.
2.Bronchial asthma , COPD.
3.Renal dysfunction, Liver dysfunction, Bleeding diathesis.
4.Psychological disorder.
5.Morbid obesity.
6.Laparoscopic cholecystectomy converted to open cholecystectomy intraoperatively.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method To assess:- <br/ ><br> Requirement of IV fentanyl intraoperatively <br/ ><br> VAS in the immediate postoperative period (15 minutes). <br/ ><br>Timepoint: To assess:- <br/ ><br> Requirement of IV fentanyl intraoperatively <br/ ><br> VAS in the immediate postoperative period (15 minutes). <br/ ><br>trail study period 18 months <br/ ><br>
- Secondary Outcome Measures
Name Time Method Duration of effective analgesia. [ From the end of surgery till the time patient requires the 1st postoperative analgesic ] <br/ ><br>Requirement of analgesics in the postoperative period in 24 hoursTimepoint: Duration of effective analgesia. [ From the end of surgery till the time patient requires the 1st postoperative analgesic ] <br/ ><br>Requirement of analgesics in the postoperative period in 24 hours <br/ ><br>trial study period 18 months