Spinal anesthesia in patients with cesarean sectio
Phase 2
- Conditions
- Spinal Anesthesia in pregnant patient.094-099
- Registration Number
- IRCT201701277745N6
- Lead Sponsor
- Deputy of Research and Technology
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete
- Sex
- Female
- Target Recruitment
- 150
Inclusion Criteria
Inclusion: Pregnant mothers who come to the operating room for non-emergency surgery to undergo surgery.
Exclusion: Patients with a history of diabetes, addiction, high blood pressure or antihypertensive drug use, and also at the time of surgery for maintaining hemodynamic status using drugs that increase blood pressure and heart rate
Exclusion Criteria
Not provided
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Heart rate and blood pressure. Timepoint: The patient's arrival time to the operating room, before the spinal anesthesia, every 10 minutes of badness for spinal anesthesia up to 60 minutes. Method of measurement: Using a blood pressure monitor and heart rate monitor.
- Secondary Outcome Measures
Name Time Method Satisfaction and a pleasant feeling by the mother. Timepoint: After the surgery and recovery time. Method of measurement: The question of patient.