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Clinical Trials/IRCT2013080514275N1
IRCT2013080514275N1
Completed
Phase 2

Comparison of sub-lingual misoprostol and intravenous oxytocin in controlling of hemorrhage after cesarean section.

Vice Chancellor for Research of Semnan University of Medical Sciences0 sites100 target enrollmentTBD

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
Postpartum hemorrhage.
Sponsor
Vice Chancellor for Research of Semnan University of Medical Sciences
Enrollment
100
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

No summary available.

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

Investigators

Sponsor
Vice Chancellor for Research of Semnan University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • singleton pregnant women; elective cesarean delivery; Gravid 1, 2 (maximum one section)
  • Exclusion criteria: Patients with preeclampsia (high blood pressure and protein in the urine); diseases cardiovascular diseases; asthma; uterine rupture; uterine leiomyoma or a women with a history of excessive bleeding after childbirth.

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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