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Clinical Trials/IRCT201304157695N3
IRCT201304157695N3CompletedPhase 1

Comparison the Hemodynamic Effects of Spinal Anesthesia with Bupivacaine-Fentanyl in Pre-eclamptic Versus Normal Pregnant women

Vice-Chancellor for Research of Qazvin University of Medical Sciences0 sites70 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
Phase 1
Status
Completed
Sponsor
Enrollment
70

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 with age range of 18-45 years old
  • Exclusion criteria:
  • Patient refusal of spinal anesthesia, presence of: fetal distress, convulsion, pulmonary edema, headache, visual impairment, impaired consciousness, coagulopathy, high systemic blood pressure (BP>170/110), systemic involvement (diabetes mellitus, chronic hypertension), positive history of antihypertensive drugs consumption

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Vice-Chancellor for Research of Qazvin University of Medical Sciences

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