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Clinical Trials/IRCT201101275709N1
IRCT201101275709N1Completed未知

Comparing the hemodynamic effects of spinal anesthesia in cesarean section of severely preeclamptic patients and healthy parturients

Hamedan University of Medical Scienece-Research Vice Chancellorship0 sites80 target enrollmentStarted: TBDLast updated:
Conditions

Trial Snapshot

Phase
未知
Status
Completed
Sponsor
Enrollment
80

Study Overview

Brief Summary

No summary available.

Study Design

Study Type
Interventional

Eligibility Criteria

Ages
14 years to 45 years (—)
Sex
Female

Inclusion Criteria

  • pregnant women with severe pre-eclamsia and healthy parturients who are candidate for termination of pregnancy with cesarean section
  • Exclusion criteria: Presence of coagulopathy (platelet less than 50000); placental abruption; severe fetal distress; history of allergy to local anesthetics; skin infection of injection site and no satisfaction of patients for regional anesthesia

Exclusion Criteria

  • Not provided

Investigators

Sponsor
Hamedan University of Medical Scienece-Research Vice Chancellorship

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