To decrease the pain during induction of general anaesthesia using Propofol (Induction agent) injection in operation theatre.
Phase 2
Completed
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2022/01/039506
- Lead Sponsor
- Rajendra Institute of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 72
Inclusion Criteria
Patients who are posted for laparoscopic cholecystectomy of ASA 1 & 2 status between the age of 20-70 years.
Exclusion Criteria
Patients not willing to consent, history of hypersensitivity to drug, past history of burn injuries/chemotherapy/radiotherapy, laparoscopic surgeries converted to open surgeries, if drugs other than study drug used for alleviation of Propofol.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Comparison of intravenous Ondansetron vs Dexamethasone as pre-treatment drugs to prevent Propofol induced pain in patients undergoing laparoscopic cholecystectomy.Timepoint: 0 mins, 1st min after injection of Propofol, 3rd min after injection which is before intubation, 5th minute after injection which is after intubation.
- Secondary Outcome Measures
Name Time Method To compare the effect of intravenous Ondansetron vs Dexamethasone as pre-treatment drugs to prevent postoperative nausea & vomiting after laparoscopic surgeries.Timepoint: Within 12 hrs