IRCT20120915010841N18
Recruiting
Phase 1
Evaluation of Efficacy of intravenous Atropine in prevention of post spinal hypotension and bradycardia in cesarean section.
Overview
- Phase
- Phase 1
- Intervention
- Not specified
- Conditions
- Spinal anesthesia in cesarean section.
- Sponsor
- Hamedan University of Medical Sciences
- Enrollment
- 88
- Status
- Recruiting
- Last Updated
- 6 years ago
Overview
Brief Summary
No summary available.
Investigators
Eligibility Criteria
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
Outcomes
Primary Outcomes
Not specified
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To check the effect of intravenous atropine in patients undergoing elective caesarean section for treating nausea and vomiting associated with spinal anaesthesiaCTRI/2023/11/059735Dr Jai Prakash Sharma