Efficacy of intravenous Atropine in prevention of post spinal hypotension and bradycardia in cesarean section.
Phase 1
Recruiting
- Conditions
- Spinal anesthesia in cesarean section.Single liveborn infant, delivered by cesareanZ38.01
- Registration Number
- IRCT20120915010841N18
- Lead Sponsor
- Hamedan University of Medical Sciences
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- Female
- Target Recruitment
- 88
Inclusion Criteria
Satisfaction to participate in the project
Pregnant women aged 18 to 46
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
Multiple pregnancies
HR resting more than 100 in minutes,
Beta-blocker intake
Study & Design
- Study Type
- interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Hypotension. Timepoint: Every two minutes to 10 minutes, then every 5 minutes to 15 minutes, then every 10 minutes until the end of the surgery. Method of measurement: Non-invasive blood pressure.;Bradycardia. Timepoint: Every two minutes to 10 minutes, then every 5 minutes to 15 minutes, then every 10 minutes until the end of the surgery. Method of measurement: Pulse Oximetry.
- Secondary Outcome Measures
Name Time Method ausea & vomiting. Timepoint: after delivery. Method of measurement: Observation.