A Comparative study on postoperative nausea and vomitting in patients undergoing laparsocopic surgeries.
Not Applicable
Not yet recruiting
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/064564
- Lead Sponsor
- Dr. Priyanka Prasannan
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Not Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
1. ASA Physical status I and II.
2. Elective Laparoscopic surgeries requiring general anaesthesia with endotracheal intubation and controlled ventilation.
3. Patients willing to give informed consent.
Exclusion Criteria
1. ASA Physical status III and IV.
2. Patients with emetic episodes in the 24 hours prior to surgery.
3. Pregnancy or lactating mothers.
4. Emergency surgeries.
5. Patients with history of smoking or PONV or motion sickness.
6. Patients on medications that cause QT. Prolongation
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative nausea and vomitingTimepoint: 0-2 hours, 2-6 hours, 6-24 hours, 24-48 hours
- Secondary Outcome Measures
Name Time Method Post-operative vitalsTimepoint: 30mins,60mins,90 mins,120 mins,3rd hour,4th hour,5th hour,6th hour,8th hour,12th hour,16th hour,20th hour,24th hour,28th hour,32nd hour,36th hour,40th hour,44th hour,48th hour