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
| Type | Name | Description |
|---|---|---|
| DRUG | Tranexamic acid | 1g tranexamic acid mixed in 100mL saline or lactated ringer |
| DRUG | Placebo | 100mL 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
- FDA-regulated drug study
Source: ClinicalTrials.gov record NCT04651166. Inclusion in this directory is not an endorsement.