Evaluation of intravenous Propofol and Midazolam on sedation during spinal anesthesia in cesarean sectio
Phase 2
Recruiting
- Conditions
- T88.52sedation and nausea & vomiting during spinal anesthesia in cesarean section.Failed moderate sedation during procedure
- Registration Number
- IRCT20120915010841N21
- Lead Sponsor
- Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 102
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
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Sedation. Timepoint: We record ramsy sedation score in 24 hours after surgery.?. Method of measurement: Ramsy sedation score.;Nausea & vomiting. Timepoint: After surgery. Method of measurement: Observation.
- Secondary Outcome Measures
Name Time Method Systolic and Diastolic Blood Pressure. Timepoint: Every 5 minutes (from drug administration until end of surgery). Method of measurement: Non-invasive automatic barometric device.;Heart Rate. Timepoint: Every 5 minutes (from drug administration until end of surgery). Method of measurement: Using a pulse oximeter.