A clinical trial comparing the preventive effect of Ondansetron and Dexamethasone on control of headache caused by local anesthetic from the lumbar in non-emergency cesarean sectio
Phase 2
- Conditions
- elective cesarean section.Delivery by elective caesarean section
- Registration Number
- IRCT20170802035464N2
- Lead Sponsor
- Arak University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
Informed consent
Elective repeated (second) cesarean section
Candidate ?cesarean with spinal anesthesia
Exclusion Criteria
Lack of consent
Candidate cesarean with general anesthesia
Drug allergy
Emergency cesarean section
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Headache. Timepoint: 12, 24 and 48 hours after cesarean. Method of measurement: Visual Analogue Scale of pain.
- Secondary Outcome Measures
Name Time Method Blood pressure. Timepoint: Every 15 minute until end of recovery. Method of measurement: Sphygmomanometer (millimeter Hg).;Heart rate. Timepoint: Every 15 minute until end of recovery. Method of measurement: Beat in minute.