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Clinical Trials/IRCT201204079399N1
IRCT201204079399N1
Completed
Phase 2

A placebo-controlled clinical trial to assess efficacy of tranexamic acid in reducing hemorrhage after vaginal delivery

Vice chancellor for research ,Kashan University of Medical Sciences0 sites200 target enrollmentTBD
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Conditionspostpartum hemorrhage.Haemorrhage following delivery of placenta

Overview

Phase
Phase 2
Intervention
Not specified
Conditions
postpartum hemorrhage.
Sponsor
Vice chancellor for research ,Kashan University of Medical Sciences
Enrollment
200
Status
Completed
Last Updated
8 years ago
OverviewInvestigatorsEligibility CriteriaOutcomesSimilar Trials

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 ,Kashan University of Medical Sciences

Eligibility Criteria

Inclusion Criteria

  • •1\- inclusion criteria:
  • •\- women with term, singleton pregnancy candidate for the first vaginal delivery
  • •\-No history of sever medical complications involving the heart,brain ,kidney
  • •\- No history of allergy to tranexamic acid
  • •\-No history of visual problem
  • •\-No history of sever pregnancy complications such as preeclampsia
  • •\-No history of thromboembolic events
  • •2\- exclusion criteria:
  • •\-patient avoidance
  • •\-placenta abruption

Exclusion Criteria

  • Not provided

Outcomes

Primary Outcomes

Not specified

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