Post operative pain comparison in patients undergoing elective laparoscopic surgery who is receving fentanyl and the patients who is receiving dexmedetomidine
Not Applicable
- Registration Number
- CTRI/2021/01/030301
- Lead Sponsor
- JSS MEDICAL COLLEGE AND HOSPITA
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
Patients of ASA physical status class 1 and 2 aged 20-60 years undergoing elective laparoscopic surgeries lasting for <2 hours
Exclusion Criteria
Pregnant, breast feeding women, hepatic, renal or cardiac insufficiency, psychiatric disease, allergy or contraindicated to study drugs, BMI >30, Obstructive sleep apnoea syndrome.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Amount of post-operative pain intensity in terms of visual analogue score (VAS) and rescue analgesics requirementsTimepoint: starting of general anaesthesia till twenty four hours after completion of surgery.
- Secondary Outcome Measures
Name Time Method 1. Assessment of intraoperative haemodynamic stability. <br/ ><br>2. Post-operative recovery status. <br/ ><br>3. Post-operative sedation in terms of Ramsay-sedation scoring system. <br/ ><br>4. Incidence of post-operative nausea and vomiting. <br/ ><br>Timepoint: starting of general anaesthesia till twenty four hours after completion of surgery.