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Trials / Completed

CompletedNCT04651166

Effect of Prophylactic Tranexamic Acid on Bleeding Outcomes for Dilation and Evacuation

Status
Completed
Phase
Phase 2
Study type
Interventional
Enrollment
48 (actual)
Sponsor
University of Hawaii · Academic / Other
Sex
Female
Age
14 Years
Healthy volunteers
Accepted

Summary

Prophylactic tranexamic acid has shown been shown to reduce maternal mortality from postpartum hemorrhage with no adverse effects, but has not been studied to reduce bleeding complications with dilation and evacuation (D\&E). We propose a randomized, double-blinded, placebo-controlled pilot study to determine whether routine use of intravenous (IV) tranexamic acid will decrease the need for interventions to control bleeding at the time of D\&E at 16 to 24 weeks gestation.

Conditions

Interventions

TypeNameDescription
DRUGTranexamic acid1g tranexamic acid mixed in 100mL saline or lactated ringer
DRUGPlacebo100mL saline or lactated ringers

Timeline

Start date
2022-02-15
Primary completion
2023-07-27
Completion
2023-07-27
First posted
2020-12-03
Last updated
2023-09-06

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT04651166. Inclusion in this directory is not an endorsement.

Effect of Prophylactic Tranexamic Acid on Bleeding Outcomes for Dilation and Evacuation (NCT04651166) · Clinical Trials Directory