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Vitamin K
Vitamin K2 (menaquinone-7; 360-mcg/d) for Cardiovascular Disease
N/A
Waitlist Available
Led By Norman K Pollock, PhD
Research Sponsored by Augusta University
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up change from baseline to 8 weeks
Awards & highlights
Study Summary
This trial is testing whether vitamin K supplementation can help improve vascular function in people with end-stage renal disease who are undergoing hemodialysis.
Eligible Conditions
- Cardiovascular Disease
- Vitamin K Deficiency
- Renal Disease
- Hemodialysis
- Chronic Kidney Disease
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ change from baseline to 8 weeks
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~change from baseline to 8 weeks
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Flow-Mediated Dilation (FMD)
Pulse Wave Velocity (PWV)
Secondary outcome measures
Prothrombin Time
Trial Design
2Treatment groups
Experimental Treatment
Placebo Group
Group I: Vitamin K2 (360-mcg/d)Experimental Treatment1 Intervention
The experimental group will take four 90-mcg of vitamin K2 (menaquinone-7; 360-mcg) softgel capsules every day for 8 weeks.
Group II: Placebo-ControlPlacebo Group1 Intervention
The placebo-control group will take four placebo softgel capsules (similar in taste and appearance to the vitamin K2 supplements) every day for 8 weeks.
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Who is running the clinical trial?
Augusta UniversityLead Sponsor
210 Previous Clinical Trials
84,968 Total Patients Enrolled
Norman K Pollock, PhDPrincipal InvestigatorAugusta University
1 Previous Clinical Trials
30 Total Patients Enrolled
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