Comparison of crystalloid with colloid in sensory level induced by spinal anesthesia in cesarean sectio
Phase 3
Recruiting
- Conditions
- Hypotension due to drugs.Hypotension due to drugsI95.2
- Registration Number
- IRCT20120910010800N10
- Lead Sponsor
- Shahid Beheshti University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 120
Inclusion Criteria
singleton pregnancy
Elective cesarean section
Gestational age more than 36 weeks
Height more than 150 and less than 175 cm
Body mass index less than 35 kg/m2
Consent to study
Exclusion Criteria
Sensitivity to local anesthetics
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method The sensory level obtained after spinal anesthesia. Timepoint: Every 5 to 30 minutes after spinal anesthesia and then at 60 and 90 minutes. Method of measurement: The sensory level will be assessed along the midline of the abdomen from T12 towards the patient's head with a blunt needle.
- Secondary Outcome Measures
Name Time Method Hypotension after spinal anesthesia. Timepoint: Throughout the operation in 5-minute intervals to 30 minutes, then in 10-minute intervals until the end of the operation. Method of measurement: Standard blood pressure monitoring.