Clinical TrialID 5539
Fearon Algorithm in Warfarin Patient Self-Management
NCT03911661
Atrial Fibrillation|Venous Thromboses|Heart Valve Diseases
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 5539
- Evidence Id
- 5539
- Core Evidence Id
- 5539
- Source Clinical Trial Id
- 5521
- Herb2 Clinical Trial Id
- HBCT005521
- Nct Id
- NCT03911661
- Title
- Fearon Algorithm in Warfarin Patient Self-Management
- Status
- Completed
- Phase
- Study Result
- No
- Study Condition
- Atrial Fibrillation|Venous Thromboses|Heart Valve Diseases
- Study Type
- Interventional
- Study Design
- Allocation: NON_RANDOMIZED|Intervention Model: CROSSOVER|Masking: NONE|Primary Purpose: TREATMENT
- Intervention
- OTHER: Fearon warfarin dosing algorithm|OTHER: Usual care
- Intervention Allocation
- Non_Randomized
- Intervention Model
- Crossover
- Intervention Mask
- Intervention Purpose
- Treatment
- Gender
- All
- Age
- Adult, Older_Adult
- Enrollment
- 30
- Outcome Measure
- Participant time spent in therapeutic INR range, Estimated time patient's INR is within their specified target range, 6-12 months|Participant percent of INRs in the therapeutic INR range, Actual proportion of measured INR within participant's specified target range, 6-12 months|Number of participant's INR results resulting in a warfarin dose change, Proportion of participant's measured INRs that result in warfarin dose being changed, 6-12 months
- Sponsor Collaborator
- University of Utah|Roche Diagnostics GmbH
- Funded By
- OTHER
- Location
- University of Utah Thrombosis Center, Salt Lake City, Utah, 84112, United States
- Other Id
- 115634
- Start Date
- 2018-11-20
- Primary Completion Date
- 2021-12-30
- Completion Date
- 2021-12-31
- First Posted
- 2019-04-11
- Results First Posted
- Last Update Posted
- 2023-05-17
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT03911661
- Title Cn
- Title En
- Fearon Algorithm in Warfarin Patient Self-Management
- Bilingual Status
- semi_complete