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Clinical Trials/IRCT20191007045023N1
IRCT20191007045023N1CompletedPhase 3

Comparison of the Effect of Phenylephrine Prophylactic Infusion with Placebo Group on Hypertension and Nausea and Vomiting of Pregnant Women During Cesarean Section Under Spinal Anesthesia

Iran University of Medical Sciences0 sites120 target enrollmentStarted: TBDLast updated:

Trial Snapshot

Phase
Phase 3
Status
Completed
Enrollment
120

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
18 years to 45 years (—)
Sex
Female

Inclusion Criteria

  • Pregnant women 18-45 years
  • Pregnant women candidates for cesarean section by spinal anesthesia
  • ASA Class 1 and 2
  • Elective cesarean section

Exclusion Criteria

  • history of allergy to phenylephrine
  • BMI>30 Kg/M2
  • hypertension (>140/90 mmHg)
  • contraindication for spinal anesthesia
  • severe cardiovascular disease
  • prematurity
  • emergency cesarean section
  • inadequate analgesia after spinal anesthesia

Investigators

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