Effect of Ondansetron and Granisetron For The Prevention Of Pruritus In Patients Undergoing Cesarean Sectio
Not Applicable
- Conditions
- Pruritus.Pruritus, unspecified
- Registration Number
- IRCT2014092219252N1
- Lead Sponsor
- Ahwaz Jondishapour University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 90
Inclusion Criteria
Women undergoing elective cesarean section with spinal anesthesia. Exclusion criteria: Drug addiction; history of allergy to ondansetron, granisetron and morphine; electrolyte abnormalities; history of pruritic skin diseases and other systemic diseases.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Pruritus. Timepoint: 3, 6 and 18 hour after intrathecal morphine. Method of measurement: visual analog scale.
- Secondary Outcome Measures
Name Time Method