Ondansetron effect in cesarea
Phase 2
- Conditions
- Spinal anesthesia.Other complications of spinal and epidural anaesthesia during pregnancy
- Registration Number
- IRCT201111138090N1
- Lead Sponsor
- Research vice Chancellorship, Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 102
Inclusion Criteria
pregnant healthy women who are candidate for elective cesarean section with spinal anesthesia. Exclusion criteria: motion sickness; hypertension; weight greater than 100kg; hepatic disease; migraine; allergy to ondansetron group drugs, using drugs that effect blood pressure or heart rate or serotonin receptor.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Bradycardia. Timepoint: Every 3 min till 10 min after anesthesia then every 5 min. Method of measurement: Heart rate per minute, automatic monitoring.;Hypotension. Timepoint: Every 3min till 10min after anesthesia, then every 5min till minute 30. Method of measurement: mmHg, automatic.
- Secondary Outcome Measures
Name Time Method Itching. Timepoint: Every 10 minute after anesthesia till minute 30. Method of measurement: Question from patient, scoring: 0 no- 1 mild- 2 severe (need to treat).;Nausea and vomiting. Timepoint: Every 10 minute after anesthesia till minute 30. Method of measurement: Question from patient, scoring: 0 no- 1 yes.;Mean consumed ephedrine. Timepoint: After anesthesia until end of operation. Method of measurement: Milligram.