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
| Type | Name | Description |
|---|---|---|
| DRUG | Tranexamic acid injection | Active group will receive 1gm Tranexamic acid 12 hourly for 48 hours |
| OTHER | Glucose 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.