It is a study to compare the effectiveness of two anaesthesia techniques in reducing postoperative nausea and vomiting in female patients undergoing laparoscopic surgery using propofol in one and combination of propofol and sevoflurane as maintenance agents in another
Phase 4
Completed
- Conditions
- Health Condition 1: K808- Other cholelithiasis
- Registration Number
- CTRI/2019/09/021449
- Lead Sponsor
- Department of anaesthesiology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- Not specified
- Target Recruitment
- 70
Inclusion Criteria
female patients belonging to American society of anaesthesiologists (ASA) physical status I or II, scheduled for laparoscopic surgery and requiring endotracheal intubation will be included in the study
Exclusion Criteria
Patients with:
1. Obesity (BMI >30kg/m.m)
2. history of nausea and vomiting or motion sickness
3. history of gastro-esophageal reflux disease
4. history of anti-emetic use in last 2 weeks before surgery
5. history of smoking or alcohol use
6. refusal to participate in study
will be excluded from the study
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method