Atrial Fibrillation Clinical Trial
— VISTAOfficial title:
Vitamin K Supplementation to Improve INR Stability in Patients on Hemodialysis Taking Warfarin for Atrial Fibrillation
| Verified date | May 2016 |
| Source | University Health Network, Toronto |
| Contact | n/a |
| Is FDA regulated | No |
| Health authority | |
| Study type | Interventional |
The purpose of this study is to determine whether vitamin K supplementation will improve anticoagulation control in patients on hemodialysis taking warfarin for atrial fibrillation. Patients who participate will receive vitamin K1 three times a week on dialysis days for a period of four months. INR levels collected during this period will be compared to the four month period prior to receiving the vitamin K1 to determine if vitamin K improves the standard deviation of INRs and time in therapeutic range.
| Status | Completed |
| Enrollment | 3 |
| Est. completion date | December 18, 2017 |
| Est. primary completion date | December 18, 2017 |
| Accepts healthy volunteers | No |
| Gender | All |
| Age group | 18 Years and older |
| Eligibility |
Inclusion Criteria: - greater than 18 years of age - Receiving in-house hemodialysis for at least 6 months - Previously diagnosed with atrial fibrillation - On warfarin for at least 6 months with a target INR of 2-3 Exclusion Criteria: - are unable to provide informed consent - have a mechanical heart valve - are receiving supplements containing vitamin K - have a known hypersensitivity to vitamin K |
| Country | Name | City | State |
|---|---|---|---|
| Canada | University Health Network | Toronto | Ontario |
| Lead Sponsor | Collaborator |
|---|---|
| University Health Network, Toronto |
Canada,
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* Note: There are 25 references in all — Click here to view all references
| Type | Measure | Description | Time frame | Safety issue |
|---|---|---|---|---|
| Primary | INR stability (standard deviation of INR values) | standard deviation of INR values, 4 months before and 4 months after the intervention | 4 months before and 4 months after intervention | |
| Secondary | Time in Therapeutic Range (Percentage of time INR levels within range) | , 4 months before and 4 months after the intervention | 4 months before and 4 months after intervention | |
| Secondary | Adverse events | Number and types of thromboembolic and bleeding complications, 4 months before and 4 months after the intervention | 4 months before and 4 months after intervention |
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