Postoperative nausea and vomiting after cesarean delivery
Phase 2
- Conditions
- Postoperative nausea and vomiting.Anaesthetic, unspecified
- Registration Number
- IRCT201201308877N1
- Lead Sponsor
- Isfahan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 132
Inclusion Criteria
patients with ASA I; age between 18 to 45 years old; scheduled for elective cesarean delivery under spinal anesthesia and signing written informed consent to participate in the present study. Exclusion criteria: patients who had smoking habit; obstetric complications or any evidence of fetal compromise; patients who had history of motion sickness; previous postoperative emesis; gastrointestinal disease or administration of antiemetic medication in the previous 24 hours; having allergy to the study drugs and any contraindication for spinal anesthesia.
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Postoperative nausea and vomiting. Timepoint: Half an hour afer Intevention. Method of measurement: Visual analogous scale(VAS).
- Secondary Outcome Measures
Name Time Method Sedation. Timepoint: Half, 2,4 and 24 hours after intervention. Method of measurement: Ramsay sedation scale.