Comparison of different antiemetics for prevention of vomiting after laparoscopic surgery
Not Applicable
- Conditions
- Health Condition 1: null- undergoing laparoscopic abdominal surgery
- Registration Number
- CTRI/2014/11/005214
- Lead Sponsor
- PGIMER
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Open to Recruitment
- Sex
- Not specified
- Target Recruitment
- 120
Inclusion Criteria
120 female patients of ASA physical status 1-2 between 19-60 yr of age scheduled to undergo day care laparoscopic gynaecological procedure
Exclusion Criteria
Patients with gastrointestinal diseases, smokers, past history of motion sickness, having BMI more than 30 kg/m2
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the incidence and severity of postoperative nausea and vomitingTimepoint: at 6 hr, 24 hr and 72 hr postoperatively
- Secondary Outcome Measures
Name Time Method Requirement of rescue anti emetic and adverse effectsTimepoint: at 6 hr, 24 hr and 72 hr postoperatively