Effect of atropine vs. ondansetron in preventing nausea and vomiting
Phase 3
Recruiting
- Conditions
- ausea and vomiting.Nausea and vomiting
- Registration Number
- IRCT20160825029520N4
- Lead Sponsor
- eyshabour University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 142
Inclusion Criteria
Age: 18-45 years old
Elective surgery
Not history of severe nausea and vomiting during pregnancy
Complete NPO time
Not taking anti-nausea medication before surgery
Exclusion Criteria
Heart rate less than 50 or more than 100 during operation
History of allergy to the drug that used in this study
History of digestive diseases
Failed Spinal Anesthesia
Bleeding more than 500 cc during surgery
Prolonged QT interval
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Severity of Nausea and Vomiting. Timepoint: Before spinal/ after spinal/ before surgery/ after the umbilical cord clamp/ after surgery/ entering the recovery/ leaving the recovery. Method of measurement: Bellville Nausea and Vomiting scoring scale.
- Secondary Outcome Measures
Name Time Method Blood pressure. Timepoint: Before spinal/ after spinal/ before surgery/ after the umbilical cord clamp/ after surgery/ entering the recovery/ leaving the recovery. Method of measurement: Anesthesia monitoring.;Heart rate. Timepoint: Before spinal/ after spinal/ before surgery/ after the umbilical cord clamp/ after surgery/ entering the recovery/ leaving the recovery. Method of measurement: Anesthesia monitoring.;Temperature. Timepoint: Before spinal/ after spinal/ before surgery/ after the umbilical cord clamp/ after surgery/ entering the recovery/ leaving the recovery. Method of measurement: Tympanic membrane thermometers.