CompletedNot Applicable

Tranexamic Acid as an Intervention in Placenta Previa

Iraq146 participantsStarted 2022-12-10

Plain-language summary

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

Who can participate

Age range

18 Years – 45 Years

Sex

FEMALE

See this in plain English?

AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Pregnant at 28 weeks gestation and more * Vaginal bleeding due to placenta previa * Stable hemodynamically * Accept to participate in the trial Exclusion Criteria: * Hypersensitivity to tranexamic acid * Acquired defective color vision * History of venous thromboembolism * Pre-existing medical conditions (diabetes mellitus, hypertension, renal disease) * Smokers * Refused to participate in the trial

Questions worth asking your doctor

Bring these to your next appointment. They're a starting point for a shared conversation — not a sign you qualify or a recommendation to enrol.

1Based on my diagnosis and history, is this trial worth exploring for me — or is there a standard treatment we should try first?
2What does this trial's phase tell us about how much is already known about its safety and benefit?
3What would taking part actually involve for me — visits, tests, time, and travel?
4What are the known and possible risks or side effects I should weigh, and how would they be monitored?
5If this trial isn't the right fit, what other options or trials would you suggest I look into?

Generated to help you prepare — always confirm anything about your own eligibility and care with the study team and your doctor.

Questions for the trial coordinator

The trial coordinator is the person who runs the study day to day. These cover the practical side — logistics, costs, and what taking part would actually mean for your life. The study team confirms whether you meet the criteria; these are questions to ask, not a sign you qualify.

1What does taking part actually involve week to week — how many visits, where, and how long does each one take?
2What costs are covered by the study, and what might I have to pay for myself, including travel, parking, or time off work?
3What happens during screening, and what happens if the study team confirms I don't meet the criteria after those tests?
4Who pays for the scans, blood work, and other tests the trial requires — the study, my insurance, or me?
5How will being in the trial affect my regular care, and will my own doctor stay informed and involved?
6Can I leave the trial at any point if I change my mind, and what would happen to my care if I do?

A starting point for the conversation — always confirm anything about your own eligibility, costs, and care with the study team and your doctor.

What they're measuring

To stope or decrease vaginal bleeding

Timeframe: Up to time of delivery

Prolong pregnancy to 36 weeks

Timeframe: Up to delivery of the fetus

Favorable perinatal outcome

Timeframe: 7 days post partum

Trial details

NCT IDNCT05688111

SponsorHawler Medical University

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2023-12-03

View on ClinicalTrials.gov More Interventional Drug in Placenta Previa trials