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Role of Extrarenal 1-Alpha-Hydroxylase in Patients With End Stage Renal Disease

Primary Purpose

End-Stage Renal Disease

Status
Completed
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Cholecalciferol
Sponsored by
University of Kansas
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for End-Stage Renal Disease focused on measuring Endstage renal disease, Vitamin D, Monocyte function

Eligibility Criteria

21 Years - 88 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • End-stage renal disease undergoing maintenance hemodialysis at KUMC outpatient hemodialysis unit
  • Dialysis vintage of at least 6 months duration
  • Nutritional vitamin D deficiency, defined as 25(OH)D <25 ng/ml
  • Age 21 to 88 years

Exclusion Criteria:

  • Active infection
  • Recent hospitalization for acute illness (within last 1 month)
  • Refusal to study participation
  • Poorly controlled secondary hyperparathyroidism (iPTH>500)
  • History of chronic inflammatory disease process, such as inflammatory bowel, rheumatoid arthritis, lupus, etc.
  • Cinacalcet therapy
  • Previous allergy to ergocalciferol
  • History of parathyroidectomy
  • Current treatment with immunosuppressant medications
  • Noncompliance with prescribed hemodialysis regimen (i.e. skipping treatments, ending sessions early)
  • Functional renal transplant within the last five years

Sites / Locations

    Arms of the Study

    Arm 1

    Arm Type

    Experimental

    Arm Label

    1

    Arm Description

    Cholecalciferol (Vitamin D)

    Outcomes

    Primary Outcome Measures

    Change in Monocyte VDR Expression With Vitamin D Therapy
    Monocytes will be analyzed pre- and post-cholecalciferol by flow cytometry to measure changes in monocyte VDR expression. Unit of measure is represented by mean florescence intensity (MFI), which is a relative measure.

    Secondary Outcome Measures

    Full Information

    First Posted
    May 12, 2008
    Last Updated
    April 10, 2014
    Sponsor
    University of Kansas
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00677534
    Brief Title
    Role of Extrarenal 1-Alpha-Hydroxylase in Patients With End Stage Renal Disease
    Official Title
    Exploring the Role of Extrarenal 1-Alpha-Hydroxylase in Patients With End Stage Renal Disease
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    April 2014
    Overall Recruitment Status
    Completed
    Study Start Date
    May 2008 (undefined)
    Primary Completion Date
    August 2009 (Actual)
    Study Completion Date
    August 2009 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Principal Investigator
    Name of the Sponsor
    University of Kansas

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief Summary
    The goal of this study is to evaluate the role of nutritional Vitamin D deficiency as a potential contributor to the morbidity witnessed in patients with end-stage renal disease
    Detailed Description
    The goals of this study are to elucidate the function of extrarenal 1 alpha-hydroxylase activity in the setting of renal failure and to evaluate the role of nutritional vitamin D deficiency as a potential contributor to monocyte-associated inflammatory pathways in patients with end-stage renal disease (ESRD). This study will consist of patients on chronic maintenance hemodialysis three times per week who have been identified to have nutritional vitamin D deficiency. After consent for study enrollment, patients will undergo a 4 week washout period of all active vitamin D supplementation. After washout is complete, an blood sample will be obtained for baseline 25(OH)D levels and monocyte isolation for analysis by flow cytometry. Patients will then be started on cholecalciferol 50,000 IU twice weekly for 8 weeks. 25-vitamin D levels will be monitored midway through the treatment phase of the study and dosing adjusted as further described in detail within the protocol section. An additional blood sample will be drawn post-therapy for repeat 25(OH)D levels and monocyte isolation for flow cytometry analysis.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    End-Stage Renal Disease
    Keywords
    Endstage renal disease, Vitamin D, Monocyte function

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    7 (Actual)

    8. Arms, Groups, and Interventions

    Arm Title
    1
    Arm Type
    Experimental
    Arm Description
    Cholecalciferol (Vitamin D)
    Intervention Type
    Drug
    Intervention Name(s)
    Cholecalciferol
    Other Intervention Name(s)
    Vitamin D, ergocalciferol
    Intervention Description
    50,000 Units PO Twice weekly for 8 weeks
    Primary Outcome Measure Information:
    Title
    Change in Monocyte VDR Expression With Vitamin D Therapy
    Description
    Monocytes will be analyzed pre- and post-cholecalciferol by flow cytometry to measure changes in monocyte VDR expression. Unit of measure is represented by mean florescence intensity (MFI), which is a relative measure.
    Time Frame
    Change from End of Washout to Week 12

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    21 Years
    Maximum Age & Unit of Time
    88 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: End-stage renal disease undergoing maintenance hemodialysis at KUMC outpatient hemodialysis unit Dialysis vintage of at least 6 months duration Nutritional vitamin D deficiency, defined as 25(OH)D <25 ng/ml Age 21 to 88 years Exclusion Criteria: Active infection Recent hospitalization for acute illness (within last 1 month) Refusal to study participation Poorly controlled secondary hyperparathyroidism (iPTH>500) History of chronic inflammatory disease process, such as inflammatory bowel, rheumatoid arthritis, lupus, etc. Cinacalcet therapy Previous allergy to ergocalciferol History of parathyroidectomy Current treatment with immunosuppressant medications Noncompliance with prescribed hemodialysis regimen (i.e. skipping treatments, ending sessions early) Functional renal transplant within the last five years
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Jason Stubbs, MD
    Organizational Affiliation
    University of Kansas Medical Center
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    20007751
    Citation
    Stubbs JR, Idiculla A, Slusser J, Menard R, Quarles LD. Cholecalciferol supplementation alters calcitriol-responsive monocyte proteins and decreases inflammatory cytokines in ESRD. J Am Soc Nephrol. 2010 Feb;21(2):353-61. doi: 10.1681/ASN.2009040451. Epub 2009 Dec 10.
    Results Reference
    result

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    Role of Extrarenal 1-Alpha-Hydroxylase in Patients With End Stage Renal Disease

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