Dose Defining Study for the Administration of Vitamin K2 Supplements in Hemodialysis Patients
Primary Purpose
Vascular Calcification
Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
Vitamin K2 supplementation
Sponsored by
About this trial
This is an interventional prevention trial for Vascular Calcification focused on measuring Vascular calcification, Hemodialysis, Matrix Gla Protein, Vitamin K2
Eligibility Criteria
Inclusion Criteria:
- age ≥18 year
- signed informed consent
- end stage renal disease treated with chronic hemodialysis at least three times a week
Exclusion Criteria:
- coumarin treatment
- known intestinal malabsorption
- inability to take oral medication
- medical conditions with a considerable probability for death within 2 months
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
360 µg Vit K2
720 µg Vit K2
1080 µg Vit K2
Arm Description
Administration of 360 µg of Vitamin K2 thrice weekly
Administration of 720 µg of Vitamin K2 thrice weekly
Administration of 1080 µg of Vitamin K2 thrice weekly
Outcomes
Primary Outcome Measures
percentage of reduction in dp-ucMGP after 8 weeks of Vitamin K2 supplementation
this study aims at verifying whether higher doses of Vitamin K2 supplementation result in an increased reduction in dp-ucMGP
Secondary Outcome Measures
Assessment of adverse reactions associated with Vitamin K2 intake
Full Information
1. Study Identification
Unique Protocol Identification Number
NCT01675206
Brief Title
Dose Defining Study for the Administration of Vitamin K2 Supplements in Hemodialysis Patients
Official Title
Randomized Prospective Open Interventional Multi-centre Study on Finding the Optimal Dose of Vitamin K2 Supplements for Hemodialysis Patients
Study Type
Interventional
2. Study Status
Record Verification Date
August 2012
Overall Recruitment Status
Completed
Study Start Date
May 2011 (undefined)
Primary Completion Date
September 2011 (Actual)
Study Completion Date
April 2012 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Rogier Caluwe
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
This study aims at finding the optimal dose of Vitamin K2 supplementation in hemodialysis patients.
Detailed Description
During the past few years evidence is emerging for a role of Matrix Gla Protein (MGP) as one of the most powerful inhibitors of vascular calcification (Shurgers LJ et al. Thromb Haemost 2008; 100: 593-603). MGP is a Vitamin K dependent protein. This means that he presence of Vitamin K2 is required to promote the gamma-carboxylation process turning MGP in its carboxylated and active form. Recent data show that dp-uc MGP correlates well with Vitamin K status (Cranenburg CM et al. Thrombosis and Haemostasis 2010; 104/4: 811-822).
It is widely recognized that patients with renal insufficiency treated with hemodialysis are prone to accelerated vascular calcification resulting in excess cardiovascular morbidity and mortality (Goodman WG et al. N Engl J Med 2000; 342: 1478-1483).
Consequently, the administration of Vitamin K2 supplements may protect hemodialysis patients against accelerated vascular calcification by enhancing the gamma-carboxylation process of MGP. However, the optimal dose of Vitamin K2 required to achieve these results remains to be defined
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vascular Calcification
Keywords
Vascular calcification, Hemodialysis, Matrix Gla Protein, Vitamin K2
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
Participant
Allocation
Randomized
Enrollment
165 (Actual)
8. Arms, Groups, and Interventions
Arm Title
360 µg Vit K2
Arm Type
Active Comparator
Arm Description
Administration of 360 µg of Vitamin K2 thrice weekly
Arm Title
720 µg Vit K2
Arm Type
Active Comparator
Arm Description
Administration of 720 µg of Vitamin K2 thrice weekly
Arm Title
1080 µg Vit K2
Arm Type
Active Comparator
Arm Description
Administration of 1080 µg of Vitamin K2 thrice weekly
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin K2 supplementation
Primary Outcome Measure Information:
Title
percentage of reduction in dp-ucMGP after 8 weeks of Vitamin K2 supplementation
Description
this study aims at verifying whether higher doses of Vitamin K2 supplementation result in an increased reduction in dp-ucMGP
Time Frame
8 weeks
Secondary Outcome Measure Information:
Title
Assessment of adverse reactions associated with Vitamin K2 intake
Time Frame
8 weeks
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
age ≥18 year
signed informed consent
end stage renal disease treated with chronic hemodialysis at least three times a week
Exclusion Criteria:
coumarin treatment
known intestinal malabsorption
inability to take oral medication
medical conditions with a considerable probability for death within 2 months
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Rogier Caluwé, MD
Organizational Affiliation
OLV Hospital Aalst Belgium
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Bruno Van Vlem, MD, PhD
Organizational Affiliation
OLV Hospital Aalst Belgium
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
An Devriese, MD, PhD
Organizational Affiliation
AZ St.-Jan Brugge Belgium
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Stefaan Vandecasteele, MD, PhD
Organizational Affiliation
AZ St.-Jan Brugge Belgium
Official's Role
Study Chair
12. IPD Sharing Statement
Learn more about this trial
Dose Defining Study for the Administration of Vitamin K2 Supplements in Hemodialysis Patients
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