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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
Rogier Caluwe
About
Eligibility
Locations
Arms
Outcomes
Full info

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

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

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

    First Posted
    August 22, 2012
    Last Updated
    August 25, 2012
    Sponsor
    Rogier Caluwe
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    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

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    Dose Defining Study for the Administration of Vitamin K2 Supplements in Hemodialysis Patients

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