Clinical Trials Directory

Trials / Completed

CompletedNCT03778242

Tranexamic Acid in Pregnant Women Undergoing Cesarean Section.

The Adjunctive Role of Temporary Uterine Packing Combined With Topical Tranexamic Acid for Reducing Blood Loss During Hemorrhagic Cesarean Delivery: A Randomized Controlled Trial

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
180 (actual)
Sponsor
Aswan University Hospital · Academic / Other
Sex
Female
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

Purpose to evaluate the effects of topical tranexamic acid (TA) on reducing post-partum hemorrhage in pregnant women with hemorrhagic cesarean section

Detailed description

Uterine atony is the major cause of postpartum hemorrhage (PPH), accounting for up to 80% of PPH cases. PPH is the leading cause of maternal morbidity and mortality worldwide, resulting in up to 28% of maternal deaths. Therefore, inducing a rapid and effective uterine contraction following delivery is an important issue. The aim of the study is to To explore the efficacy and safety of temporary uterine packing combined with topical tranexamic acid (TA) as an adjunct for reducing blood loss during a hemorrhagic cesarean delivery (CD), compared with placebo.

Conditions

Interventions

TypeNameDescription
DRUGTopical tranexamic acidtemporary uterine packing with gauze of the dimensions soaked with 2 gm tranexamic diluted in 60ml saline acid
DRUGnormal saline2 placebo ampoules to TA in 100 ml saline by slow infusion

Timeline

Start date
2019-01-01
Primary completion
2022-03-30
Completion
2022-07-01
First posted
2018-12-19
Last updated
2023-04-04

Locations

1 site across 1 country: Egypt

Source: ClinicalTrials.gov record NCT03778242. Inclusion in this directory is not an endorsement.