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Evaluation of effect of intra venuos Tranexamic acid and Misoprostol on Post Partum Hemorrhage and side effects of hemorrhage.

Not Applicable
Completed
Conditions
Bleeding post Partum.
haemorrhage after delivery of fetus or infant
Registration Number
IRCT2012122411862N1
Lead Sponsor
Vice chanecllor for research Tabriz University of Medical Sciences
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete
Sex
Female
Target Recruitment
200
Inclusion Criteria

bleeding more than 500 mL after vaginal delivery and cesarean more than 1000 mm; willingness to participate in the study
Exclusion criteria: an acute medical or surgical conditions, including heart disease, liver, kidney and blood disorders; having allergy TXA; those who have thromboembolic disorders, women with high risk of pregnancy complications such as severe preeclampsia

Exclusion Criteria

Not provided

Study & Design

Study Type
interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Bleeding. Timepoint: First 24 hours after childbirth or surgery. Method of measurement: Physical Examination.
Secondary Outcome Measures
NameTimeMethod
The need for transfusion. Timepoint: 12 to 24 hours after delivery. Method of measurement: Questionnaire.
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