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Clinical Trial Summary

The aim of this study is to compare the effect of low dose of Tranexamic acid (1gm) and Ethamsylate (1gm) after prophylactic oxytocin administration versus placebo with prophylactic oxytocin given in the 2 minutes after child delivery in patient undergoing LSCS at high risk for post partum hemorrhage


Clinical Trial Description

Research Question:

Is the combination of Tranexamic acid and Ethamsylate is more effective than oxytocin alone for preventing postpartum hemorrhage if they are given after delivery of the fetus ? ;


Study Design

Allocation: Randomized, Endpoint Classification: Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Prevention


Related Conditions & MeSH terms


NCT number NCT02604719
Study type Interventional
Source Ain Shams University
Contact ahmed Dr alanwar, MD
Phone +201111486669
Email eladwar@hotmail.com
Status Not yet recruiting
Phase Phase 1/Phase 2
Start date November 2015
Completion date July 2016

See also
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Completed NCT02805426 - Effectiveness of Tranexamic Acid When Used as an Adjunct to Misoprostol for the Treatment of Postpartum Hemorrhage Phase 4
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Completed NCT02910310 - Introduction of UBT for PPH Management in Three Countries N/A