Last updated: May 6, 2024
Sponsor: University of Utah
Overall Status: Active - Recruiting
Phase
N/A
Condition
Venous Thromboembolism
Blood Clots
Venous Thrombosis
Treatment
Usual care provided by anticoagulation providers
Patient self-management
Clinical Study ID
NCT04766216
IRB_00141141
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- At least 18 years of age treated with warfarin for any indication for at least 9months prior to enrollment
- Demonstrate the willingness and ability to test their own INR using a home INRmonitoring device or have same-day access to clinic-derived INR results (e.g., viaelectronic medical record secure messaging)
- Willing to make independent decisions about warfarin dosing based on INR results
- Able to perform INR tests at least every 2 weeks
- Currently have and willing to maintain internet access for the duration of the studyin order to complete online data collection forms
- Have an anticipated duration of warfarin therapy of at least 6 months
Exclusion
Exclusion Criteria:
- Goal INR range other than 2.0-3.0 or 2.5-3.5
- Known poor adherence to warfarin therapy
- Non-English speaking
- Inability or refusal to provide written informed consent
Study Design
Total Participants: 150
Treatment Group(s): 2
Primary Treatment: Usual care provided by anticoagulation providers
Phase:
Study Start date:
March 15, 2023
Estimated Completion Date:
April 30, 2025
Study Description
Connect with a study center
VA Loma Linda Healthcare System
Loma Linda, California 92357
United StatesActive - Recruiting
Brigham and Women's Hospital
Boston, Massachusetts 02115
United StatesCompleted
University of Michigan
Ann Arbor, Michigan 48109
United StatesCompleted
University of Utah Thrombosis Center
Salt Lake City, Utah 84112
United StatesActive - Recruiting
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