Comparison of oral and intravenous ondansetron in the prevention of postoperative nausea and vomiting in cesarean section with spinal anesthesia
Phase 2
- Conditions
- ausea and vomiting.Nausea and vomiting
- Registration Number
- IRCT201212162080N13
- Lead Sponsor
- Arak University of Medical Sciences,Vice chancellor for research
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 162
Inclusion Criteria
age between 18-45 and ASA Class I and II
Exclusion criteria:
history of postoperative nausea and vomiting; history of motion sickness; history of allergy to ondansetron; more than two failure in spinal anaesthesia;
history of hyperemesis gravidarum.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method ausea and vomiting. Timepoint: At 0, 1, 2, 4 and 6 hours after arrive to recovery. Method of measurement: Clinical assesment.;Consciousness. Timepoint: At 0, 1, 2, 4 and 6 hours after arrive to recovery. Method of measurement: Using Ramsay score.
- Secondary Outcome Measures
Name Time Method