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
| Type | Name | Description |
|---|---|---|
| DRUG | Vitamin 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.