CI

At a glance

ClinicalIndex Comparison Record
N/ACompleted· 51 enrolled
Drug / intervention
Warfarindrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT02392104
NCT02392104N/ACompleted

Prospective Evaluation of an Extended Interval of INR Follow-up in a VA Anticoagulation Service

William S. Middleton Memorial Veterans Hospital·interventional·Posted Mar 18, 2015·Updated Dec 11, 2019

In Brief

A clinical study evaluating Warfarin for Anticoagulation. Completed, enrolled 51 participants.

Detailed Summary

The purpose of this study is to determine the feasibility, safety, and acceptability of implementing an extended interval of INR follow-up in Veterans on a stable dose of warfarin in the Anticoagulation Clinic at the William S. Middleton Memorial Veterans Hospital. All participants will be provided usual care from the anticoagulation clinic, except for the interval between INRs. If the participant continues to be on a stable dose of warfarin and the INRs are within the goal range of 2-3 (including lab variation), follow-up visits will be scheduled following an extended interval protocol. Patient satisfaction will be evaluated at various points throughout the study. Additionally provider satisfaction, confidence, and knowledge of the extended interval protocol will be analyzed. Bleeding and thromboembolic events will be evaluated to ensure the safety of an extended follow-up interval.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsAnticoagulation
Countries--

Timeline

N/ACompletedFinished
201520162017201820192020202120222023202420252026
First PostedMar 18, 2015
Enrollment StartMar 27, 2015
Primary CompletionJun 25, 2017
TodayJul 2, 2026
Enrollment to primary: 2.2 yearsPosted 11.3 years ago

Interventions

Warfarindrug

If the patient's INRs stay within goal range, their interval of INR follow-up will be extended based on a protocol to a maximum of 12 weeks.