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Anti-fibrinolytic
ProphylacticTranexamic Acid for Postpartum Hemorrhage (TXA Trial)
Phase 4
Waitlist Available
Led By Maureen E Farrell, MD
Research Sponsored by United States Naval Medical Center, San Diego
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to six weeks from date of delivery
Awards & highlights
TXA Trial Summary
Hemorrhage remains the leading cause of maternal death worldwide. Tranexamic acid has been shown to reduce rates of hemorrhage when given prophylactically prior to cesarean delivery. It has also been shown to be an effective treatment in response to hemorrhage after a vaginal delivery. The aim of this study is to assess the impact of TXA on hemorrhage rates when given prophylactically prior to all deliveries.
Eligible Conditions
- Postpartum Hemorrhage
TXA Trial Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ up to six weeks from date of delivery
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to six weeks from date of delivery
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Incidence of postpartum hemorrhage
Secondary outcome measures
Additional tranexamic acid administered
Amount of 15-methyl prostaglandin F2(PGF2) administered
Amount of methylergonovine administered
+26 moreSide effects data
From 2017 Phase 4 trial • 246 Patients • NCT020308212%
Hematoma/Seroma
100%
80%
60%
40%
20%
0%
Study treatment Arm
Epsilon-aminocaproic Acid (Amicar) - Total Hip Arthroplasty
Tranexamic Acid (TXA) - Total Hip Arthroplasty
Epsilon-aminocaproic Acid (Amicar) - Total Knee Arthroplasty
Tranexamic Acid (TXA) - Total Knee Arthroplasty
TXA Trial Design
1Treatment groups
Experimental Treatment
Group I: ProphylacticTranexamic AcidExperimental Treatment1 Intervention
Once consented, patients to receive 1000mg/10ml normal saline infusion of TXA with the delivery of the infant's anterior shoulder.
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Who is running the clinical trial?
United States Naval Medical Center, San DiegoLead Sponsor
102 Previous Clinical Trials
22,716 Total Patients Enrolled
Maureen E Farrell, MDPrincipal InvestigatorUnited States Naval Medical Center, San Diego,CA
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