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Clinical Trials/IRCT20120915010841N18
IRCT20120915010841N18
Recruiting
Phase 1

Evaluation of Efficacy of intravenous Atropine in prevention of post spinal hypotension and bradycardia in cesarean section.

Hamedan University of Medical Sciences0 sites88 target enrollmentTBD

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.

Registry
who.int
Start Date
TBD
End Date
TBD
Last Updated
6 years ago
Study Type
Interventional
Sex
Female

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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