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Antifibrinolytic Agent
Tranexamic Acid Arm (TXA) for Hip Fracture
Phase 2
Waitlist Available
Led By Brandon Yuan, MD
Research Sponsored by Mayo Clinic
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up length of hospitalization (approximately 3 to 5 days)
Awards & highlights
Study Summary
This trial will study whether tranexamic acid can help treat hip fractures.
Eligible Conditions
- Hip Fracture
- Intertrochanteric Fractures
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ length of hospitalization (approximately 3 to 5 days)
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~length of hospitalization (approximately 3 to 5 days)
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Number of Subjects Transfused at Least 1 Unit of Packed Red Blood Cells
Secondary outcome measures
(Myocardial Infarction) MI Diagnosed
All-cause Mortality
Calculated Blood Loss
+4 moreTrial Design
2Treatment groups
Active Control
Placebo Group
Group I: Tranexamic Acid Arm (TXA)Active Control1 Intervention
Subjects will be treated with early administration of TXA in the Emergency Department
Group II: Control ArmPlacebo Group1 Intervention
Subjects will be treated with a placebo in the Emergency Department
Find a Location
Who is running the clinical trial?
Mayo ClinicLead Sponsor
3,205 Previous Clinical Trials
3,766,736 Total Patients Enrolled
1 Trials studying Hip Fracture
138 Patients Enrolled for Hip Fracture
Brandon Yuan, MDPrincipal InvestigatorMayo Clinic
2 Previous Clinical Trials
70 Total Patients Enrolled
Frequently Asked Questions
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