Investigating the effect of Ondansetron on nausea and itching caused by spinal Fentanyl injectio
Phase 3
Recruiting
- Conditions
- Spinal anesthesia.
- Registration Number
- IRCT20160307026950N47
- Lead Sponsor
- Esfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
Patients 18 to 65 years old
Anesthesia class I and II according to ASA criteria
Candidate for lower limb surgery under spinal anesthesia
Informed consent to enter the study
Exclusion Criteria
History of smoking, drug and psychedelic addiction
Allergy to any anesthetic drugs, Ondansetron and fentanyl
History of coagulation disorders
High ICP
Pregnancy or breastfeeding
Skin infection at the injection site
Anti-nausea use in the last 24 hours
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of nausea. Timepoint: Every 5 minutes after spinal until 15 minutes and then every 15 minutes until the end of the 4th hour. Method of measurement: Nausea and vomiting severity behavioral scale questionnaire.;Itching scale. Timepoint: Every 5 minutes after spinal until 15 minutes and then every 15 minutes until the end of the 4th hour. Method of measurement: Itching severity scale questionnaire.
- Secondary Outcome Measures
Name Time Method