Tranexamic Acid for Reducing Blood Loss During C-Sections
Prophylactic Tranexamic Acid To Reduce Blood Loss During Caesarean Delivery.
Recruiting
N/A
Interventional Study
Post Partum Hemorrhage
At a Glance
- Age
- 18 – 45
- Sex
- Female
- Study type
- Interventional
- Purpose
- Prevention
- Participants needed
- 300 (estimated)
- Sponsor
- Aligarh Muslim University · Other
Who this trial is looking for
This trial is looking for women who are having a cesarean delivery. By joining, you will receive tranexamic acid to see if it helps reduce blood loss during the surgery.
Are You a Good Fit for This Trial?
You may be able to join if
- I am having a cesarean delivery.
- I am willing to participate in the study.
You may not be able to join if
- I am critically ill.
- I do not want to give consent to participate.
- I have a ruptured uterus.
- I am undergoing a caesarean hysterectomy.
Summarized in plain language from this trial's official eligibility criteria. The full criteria are further down this page — only the research team can confirm whether you qualify.
Think this trial could be right for you?
Answer a few quick questions to see if you may meet the eligibility requirements.
Check Your Eligibility
About This Trial
Postpartum hemorrhage continues to be the leading cause of maternal morbidity and mortality. Globally, it is responsible for 25% of all pregnancy-related deaths. PPH is unpredictable and may occur in the absence of risk factors. Tranexamic acid is an antifibrinolytic proven to reduce blood loss and transfusion requirements for various surgeries. This study aims to explore the effectiveness of tran…
Trial Locations
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Eligibility Criteria
Inclusion Criteria:
1. The women undergoing cesarean delivery (both elective and emergency) during the study period.
2. Willing to participate in the study after understanding the concept.
Exclusion Criteria:
1. Critically ill patient.
2. Not willing to give consent to participate in the study
3.…
Contacts