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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 weeks
Treatment ~ Varies
Follow Up ~length of hospitalization (approximately 3 to 5 days)
This trial's timeline: 3 weeks for screening, Varies for treatment, and length of hospitalization (approximately 3 to 5 days) for reporting.

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 more

Trial 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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~18 spots leftby Apr 2025