IRCT20120915010841N21
Recruiting
Phase 2
Comparative Evaluation of intravenous Propofol and Midazolam on sedation and nausea & vomiting during spinal anesthesia in cesarean section
Overview
- Phase
- Phase 2
- Intervention
- Not specified
- Conditions
- sedation and nausea & vomiting during spinal anesthesia in cesarean section.
- Sponsor
- Hamedan University of Medical Sciences
- Enrollment
- 102
- Status
- Recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
Inclusion Criteria
- •18\-45 aged pregnant women for C/S
- •ASA CLASS 1, 2
- •Satisfaction to participate in the project
- •Pregnant women who underwent cesarean section under spinal anesthesia
Exclusion Criteria
- •sensitivity to medications used
- •Patients who have failed spinal anesthesia and undergo general anesthesia
- •Lung disease, heart disease, asthma, fever, hypertension, preeclampsia and eclampsia, cardiac arrhythmia
- •Emergency Cesarean
- •Eclampsia and Preeclampsia
- •Multiple pregnancy
- •Spinal anesthesia contraindications (high ICP, hypovolemia, anemia, coagulation disorders, etc.)
- •History of allergy to eggs, soy, midazolam and propofol
- •Use of antiemetic drugs
Outcomes
Primary Outcomes
Not specified
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