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Effects of Oral Tranexamic Acid on Short Term Postoperative Outcomes Following Total Shoulder Arthroplasty

Phase 3
Not yet recruiting
Conditions
Shoulder Arthroplasty
Interventions
Registration Number
NCT06902714
Lead Sponsor
University of Alabama at Birmingham
Brief Summary

The purpose of this clinical trial is to evaluate the short-term clinical outcomes of patients undergoing total shoulder arthroplasty who receive an extended postoperative course of oral tranexamic acid

Detailed Description

Not available

Recruitment & Eligibility

Status
NOT_YET_RECRUITING
Sex
All
Target Recruitment
60
Inclusion Criteria
  • Skeletally mature patients (ages 18-79) undergoing primary total shoulder arthroplasty
Exclusion Criteria
  • Patients with Cancer, venous thromboembolism, stroke, heart disease, pregnant or nursing, allergic to TXA, current tobacco use, anticoagulants other than aspirin.

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
oral tranexamic acidoral tranexamic acid-
Oral PlaceboPlacebo-
Primary Outcome Measures
NameTimeMethod
VAS2 weeks

visual analog scale

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University of Alabama at Birmingham

🇺🇸

Birmingham, Alabama, United States

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