Clinical Trials Directory

Trials / Completed

CompletedNCT00287313

Daily Vitamin K in Patients on Warfarin With Unstable INRs

Use of Daily Vitamin K Supplementation in Patients on Warfarin With a History of Frequent Dose Changes or Variable INRs

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
15 (actual)
Sponsor
University of North Carolina, Chapel Hill · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine if daily Vitamin K supplementation stabilizes INRs in patients taking warfarin with a history of frequent dose changes or variable INRs.

Detailed description

Consistent daily Vitamin K intake may contribute to the stabilization of INR values in patients with unstable INRs on warfarin therapy. Subjects with unstable INRs will be identified from the existing patient records of the UNC Anticoagulation Clinics. Eligible subjects will sign an informed consent form and will receive a point-of-care (POC) INR monitoring device. They will undergo 9 weeks of home INR monitoring via the POC device (with monthly clinic follow-up). They will subsequently be provided with 500 mcg Vitamin K tablets to be taken once daily. Weekly POC INR monitoring with monthly clinic follow-up will continue for an additional 8 weeks.

Conditions

Interventions

TypeNameDescription
DRUGVitamin K

Timeline

Start date
2005-10-01
Primary completion
2006-05-01
Completion
2006-05-01
First posted
2006-02-06
Last updated
2010-01-12

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT00287313. Inclusion in this directory is not an endorsement.