Prophylactic Tranexamic Acid Use After Vaginal Delivery

Status Completed

Clinical Trial Summary

In this study, our aim was to evaluate the effectiveness of prophylactic tranexamic acid use after vaginal delivery in pregnant women aged 18-45 years and 34-42 weeks according to the risk of postpartum hemorrhage.

Clinical Trial Description

It was carried out as a double-blind prospective randomized controlled Phase 4 drug study with 480 singleton pregnant women in Bursa Yüksek İhtisas Training and Research Hospital between September 1, 2021 and February 28, 2022. The patients were divided into two groups as low risk (240 patients) and high risk (240 patients) according to their postpartum hemorrhage risks, and the patients in each group were randomly divided into two groups. Group 1: were given intravenous tranexamic acid and group 2: were given placebo. The blood loss at the 3rd and 4th stages of labor was calculated by weighing the blood collected with the help of a collecting pochette and using the estimated blood loss formula. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details

NCT number	NCT05429580
Study type	Interventional
Source	Sanliurfa Mehmet Akif Inan Education and Research Hospital
Contact
Status	Completed
Phase	N/A
Start date	September 1, 2021
Completion date	February 28, 2022

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