Clinical Trials Directory

Trials / Completed

CompletedNCT05688111

Tranexamic Acid as an Intervention in Placenta Previa

Tranexamic Acid in Pregnant Women With Placentae Previa: A Double-blind, Multicenter Randomized Clinical Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
146 (actual)
Sponsor
Hawler Medical University · Academic / Other
Sex
Female
Age
18 Years – 45 Years
Healthy volunteers
Not accepted

Summary

Antepartum hemorrhage (APH) due to placenta previa is an important cause of worldwide perinatal mortality and maternal morbidity in pregnant women

Detailed description

Antepartum hemorrhage (APH) due to placenta previa is an important cause of worldwide perinatal mortality and maternal morbidity in pregnant women. No medication is of specific benefit to a patient with placenta previa. Tocolysis may be cautiously considered in some circumstances in order to administer antenatal corticosteroids. A review article concluded that there is no improvement in perinatal outcome with prolonged tocolytics, and tocolysis beyond 48 hours is not clinically indicated.

Conditions

Interventions

TypeNameDescription
DRUGTranexamic acid injectionActive group will receive 1gm Tranexamic acid 12 hourly for 48 hours
OTHERGlucose water 5%Placebo group 30ml will be received 12 hourly for 48 hours

Timeline

Start date
2022-12-10
Primary completion
2023-12-03
Completion
2023-12-03
First posted
2023-01-18
Last updated
2025-01-27

Locations

2 sites across 1 country: Iraq

Source: ClinicalTrials.gov record NCT05688111. Inclusion in this directory is not an endorsement.