Clinical Trials Directory

Trials / Unknown

UnknownNCT02604719

Tranexamic Acid and Ethamsylate For Preventing PPH in Patient Undergoing LSCS at High Risk For PPH

Tranexamic Acid and Ethamsylate For Preventing Post Partum Hemorrhage in Patient Undergoing LSCS at High Risk For Post PartumHemorrhage : A Randomized Controlled Trial

Status
Unknown
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
64 (estimated)
Sponsor
Ahmed Alanwar · Academic / Other
Sex
Female
Age
18 Years – 35 Years
Healthy volunteers
Accepted

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

Detailed 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 ?

Conditions

Interventions

TypeNameDescription
DRUGTranexamic Acid and EthamsylateThe intervention will be the intravenous administration of 10 ml blinded vial of the study drugs (either 1 gmTranexamic acid and 1 gm Ethamsylate or placebo according to randomization group) slowly (over 30-60 sec ) in the 2 minutes after birth and the routine prophylactic oxytocin and after the cord has been clamped , all generally by the anesthesiologist or obstetrician then a pad will be placed under women buttocks then weighting the pads to allow objective measurement of blood loss.

Timeline

Start date
2015-11-01
Primary completion
2016-05-01
Completion
2016-07-01
First posted
2015-11-13
Last updated
2015-11-30

Source: ClinicalTrials.gov record NCT02604719. Inclusion in this directory is not an endorsement.