A study where vomiting after cesarean operation is compared among 3 groups who receive spinal anesthesia by 3 different drugs
Phase 3
- Conditions
- Health Condition 1: O- Medical and Surgical
- Registration Number
- CTRI/2024/03/064486
- Lead Sponsor
- Office of the Principal
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- ot Yet Recruiting
- Sex
- Not specified
- Target Recruitment
- 0
Inclusion Criteria
ASA Grade 2 patients
Patients providing valid inform consent
Patients undergoing Emergency LUCS under spinal anaesthesia
Exclusion Criteria
Patients who do not give valid consent
Patients with complicated pregnancy
Patients with coagulopathies
Patient with features of shock
Patients with local site infection
Patients with history of motion sickness
Patient with psychiatric problems or communication problems
Patients with failed spinal anaesthesia
Patients with blood pricked spinal anaesthesia
Duration of surgery more than 90 minutes
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Incidence of post operative nausea and vomiting among the study groupsTimepoint: 0, 2, 6, 12 , 24 hours after completion of surgery
- Secondary Outcome Measures
Name Time Method