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The Effects of Vitamin K2 Supplementation on the Progression of Coronary Artery Calcification (VitaK-CAC)

Primary Purpose

Coronary Artery Disease

Status
Unknown status
Phase
Not Applicable
Locations
Netherlands
Study Type
Interventional
Intervention
Menaquinone-7 (Vitamin K2)
Placebo capsules
Sponsored by
Maastricht University Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Coronary Artery Disease focused on measuring Coronary Artery Calcification, Vitamin K, Trial, Treatment

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Age 18 years or older
  • Baseline Coronary Computed Tomographic Angiography (CCTA) of sufficient quality
  • Baseline Agatston calciumscore 100 - 400

Exclusion Criteria:

  • Baseline-scan of insufficient quality
  • Heart rate greater than 70 beats per minute during first scan.(despite adequate treatment with metoprolol)
  • Chronic or paroxysmal Atrial Fibrillation
  • Presence or scheduled coronary revascularization procedure
  • History of myocardial infarction or stroke.
  • Presence of Diabetes Mellitus.
  • Known kidney disease or a Glomerular Filtration Rate (GFR)MDRD < 60 ml/min/1.73m2
  • Malignant disease (exception: treated basal-cell or squamous cell carcinoma).
  • Use of Vitamin K antagonists.
  • A life-expectancy < 2 years
  • Pregnancy or wish to become pregnant in the near future.

Sites / Locations

  • Maastricht University Medical Center

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Vitamin K2 supplementation

Placebo control

Arm Description

Outcomes

Primary Outcome Measures

Coronary Artery Calcification-score progression

Secondary Outcome Measures

Arterial Stiffness measured by Carotid-Femoral Pulse-Wave Velocity
Carotid Intima Media Thickness

Full Information

First Posted
October 26, 2009
Last Updated
September 12, 2018
Sponsor
Maastricht University Medical Center
Collaborators
VitaK
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1. Study Identification

Unique Protocol Identification Number
NCT01002157
Brief Title
The Effects of Vitamin K2 Supplementation on the Progression of Coronary Artery Calcification
Acronym
VitaK-CAC
Official Title
The Effects of Vitamin K2 Supplementation on the Progression of Coronary Artery Calcification
Study Type
Interventional

2. Study Status

Record Verification Date
September 2018
Overall Recruitment Status
Unknown status
Study Start Date
October 2011 (undefined)
Primary Completion Date
October 2019 (Anticipated)
Study Completion Date
October 2019 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Maastricht University Medical Center
Collaborators
VitaK

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Both Coronary Artery Calcification (CAC)and its annual progression are a strong predictors of cardiovascular events. The development of arterial calcification results from imbalance between calcification promoting and inhibiting factors. An important inhibitor of calcification is Matrix Gla Protein (MGP): a protein present in the vascular wall where it is synthesized by Vascular Smooth Muscle Cells (VSMC). MGP requires Vitamin K-mediated carboxylation to function properly. Deficiency of Vitamin K has been demonstrated to cause arterial calcification and a diet containing large amounts of Vitamin K2 was associated with lower CAC and cardiovascular risk. In animal studies, active supplementation of Vitamin K2 caused regression of existing arterial calcification. Therefore, the aim of this randomized, double-blind, placebo-controlled clinical trial is to investigate whether daily supplementation of Vitamin K2 (Menaquinone-7) to patients with established CAC will lead to a decreased progression-rate of CAC after 24 months of follow-up in comparison to placebo.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Coronary Artery Disease
Keywords
Coronary Artery Calcification, Vitamin K, Trial, Treatment

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
180 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Vitamin K2 supplementation
Arm Type
Experimental
Arm Title
Placebo control
Arm Type
Placebo Comparator
Intervention Type
Dietary Supplement
Intervention Name(s)
Menaquinone-7 (Vitamin K2)
Intervention Description
Menaquinone-7 (Vitamin K2)
Intervention Type
Other
Intervention Name(s)
Placebo capsules
Intervention Description
Capsules containing no Menaquinone-7
Primary Outcome Measure Information:
Title
Coronary Artery Calcification-score progression
Time Frame
12 and 24 months
Secondary Outcome Measure Information:
Title
Arterial Stiffness measured by Carotid-Femoral Pulse-Wave Velocity
Time Frame
0, 12 and 24 months
Title
Carotid Intima Media Thickness
Time Frame
0, 12 and 24 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Age 18 years or older Baseline Coronary Computed Tomographic Angiography (CCTA) of sufficient quality Baseline Agatston calciumscore 100 - 400 Exclusion Criteria: Baseline-scan of insufficient quality Heart rate greater than 70 beats per minute during first scan.(despite adequate treatment with metoprolol) Chronic or paroxysmal Atrial Fibrillation Presence or scheduled coronary revascularization procedure History of myocardial infarction or stroke. Presence of Diabetes Mellitus. Known kidney disease or a Glomerular Filtration Rate (GFR)MDRD < 60 ml/min/1.73m2 Malignant disease (exception: treated basal-cell or squamous cell carcinoma). Use of Vitamin K antagonists. A life-expectancy < 2 years Pregnancy or wish to become pregnant in the near future.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Abraham Kroon, MD, PhD
Organizational Affiliation
Maastricht University Medical Center
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Peter de Leeuw, MD, PhD
Organizational Affiliation
Maastricht University Medical Center
Official's Role
Study Chair
Facility Information:
Facility Name
Maastricht University Medical Center
City
Maastricht
ZIP/Postal Code
6202 AZ
Country
Netherlands

12. IPD Sharing Statement

Learn more about this trial

The Effects of Vitamin K2 Supplementation on the Progression of Coronary Artery Calcification

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