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Vitamin D3 for the Treatment of Low Vitamin D in Cystic Fibrosis

Primary Purpose

Cystic Fibrosis, Vitamin D Deficiency

Status
Withdrawn
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
cholecalciferol
Sponsored by
Children's Hospital of Philadelphia
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Cystic Fibrosis focused on measuring cystic fibrosis, vitamin d, inflammation

Eligibility Criteria

10 Years - 25 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. Subjects age 10-25 years
  2. cystic fibrosis
  3. 25-(OH)-D < 20 ng/mL
  4. FEV1 > 40% -

Exclusion Criteria:

  1. inability to perform pulmonary function or hand-grip tests
  2. liver disease (including cirrhosis and portal hypertension) or baseline liver enzymes 21/2-fold greater than the upper limit of normal
  3. acute use of glucocorticoids at time of testing
  4. acute pulmonary exacerbation at time of testing
  5. known non-adherence to enzyme replacement
  6. hypercalcemia
  7. engages in "suntanning

Sites / Locations

    Outcomes

    Primary Outcome Measures

    serum 25-hydroxy vitamin D levels

    Secondary Outcome Measures

    body composition
    inflammatory markers
    muscles strength

    Full Information

    First Posted
    September 26, 2008
    Last Updated
    February 19, 2010
    Sponsor
    Children's Hospital of Philadelphia
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00762918
    Brief Title
    Vitamin D3 for the Treatment of Low Vitamin D in Cystic Fibrosis
    Official Title
    Vitamin D and Its Non-Classic Roles in Cystic Fibrosis
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2010
    Overall Recruitment Status
    Withdrawn
    Why Stopped
    Recruitment
    Study Start Date
    March 2008 (undefined)
    Primary Completion Date
    September 2008 (Actual)
    Study Completion Date
    September 2008 (Anticipated)

    3. Sponsor/Collaborators

    Name of the Sponsor
    Children's Hospital of Philadelphia

    4. Oversight

    Data Monitoring Committee
    Yes

    5. Study Description

    Brief Summary
    Vitamin D deficiency is common in cystic fibrosis. Vitamin D deficiency frequently persists despite aggressive treatment with ergocalciferol, a vitamin D preparation also known as vitamin D2. Cholecalciferol, a vitamin D preparation also known as vitamin D3,may work better to increase vitamin D levels. Vitamin D is important for absorption of calcium from the diet and bone health. Vitamin D more recently has been found to play a role in regulating the normal inflammatory process. Since cystic fibrosis is a state of excessive inflammation, vitamin D may be playing a role in cystic fibrosis. We hypothesize: cholecalciferol will work better to increase vitamin D levels in patients iwth cystic fibrosis and that it will have an effect on markers of inflammation.
    Detailed Description
    Vitamin D deficiency is common in cystic fibrosis (CF) and persists despite relatively high doses of ergocalciferol, vitamin D2. Replacement has traditionally been focused upon maintenance of calcium and phosphorus homeostasis and bone health. However, non-classic roles of vitamin D have become increasingly recognized and the contribution of vitamin D deficiency to non-bone disorders has become apparent. Vitamin D deficiency has been associated with increased risk of a variety of cancers, autoimmune diseases such as Type 1 diabetes and multiple sclerosis, Type 2 diabetes, tuberculosis, and myopathy. The connection between vitamin D and these disease states likely reflects vitamin D's role as a transcriptional regulator: it participates in cell cycle regulation and in the innate immune system mediates cathelicidin production following activation of toll-like receptors.One hallmark of CF is pulmonary hyper-inflammation with recurrent infections. Additionally, malnutrition and decreased lean muscle mass threaten pulmonary function in CF. While vitamin D and its relation to bone has been explored in CF, the role of vitamin D in inflammation, lean body mass and strength, and pulmonary muscle strength has not been investigated. Moreover, vitamin D replacement has traditionally been with ergocalciferol, vitamin D2. Vitamin D3, cholecalciferol, has a longer half-life and is considered more potent. Thus, cholecalciferol treatment of children and young adults with CF and vitamin D deficiency may be useful for attaining normal vitamin D status and for exploring the impact of vitamin D upon lean body mass, pulmonary muscle strength, and inflammation.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Cystic Fibrosis, Vitamin D Deficiency
    Keywords
    cystic fibrosis, vitamin d, inflammation

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 3
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    N/A
    Enrollment
    0 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Dietary Supplement
    Intervention Name(s)
    cholecalciferol
    Other Intervention Name(s)
    Vitamin D3
    Intervention Description
    cholecalciferol 5000 IU capsule by mouth daily for 3 months
    Primary Outcome Measure Information:
    Title
    serum 25-hydroxy vitamin D levels
    Time Frame
    3 months
    Secondary Outcome Measure Information:
    Title
    body composition
    Time Frame
    3 months
    Title
    inflammatory markers
    Time Frame
    3 months
    Title
    muscles strength
    Time Frame
    3 months

    10. Eligibility

    Sex
    All
    Minimum Age & Unit of Time
    10 Years
    Maximum Age & Unit of Time
    25 Years
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Subjects age 10-25 years cystic fibrosis 25-(OH)-D < 20 ng/mL FEV1 > 40% - Exclusion Criteria: inability to perform pulmonary function or hand-grip tests liver disease (including cirrhosis and portal hypertension) or baseline liver enzymes 21/2-fold greater than the upper limit of normal acute use of glucocorticoids at time of testing acute pulmonary exacerbation at time of testing known non-adherence to enzyme replacement hypercalcemia engages in "suntanning
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Andrea Kelly, MD
    Organizational Affiliation
    Children's Hospital of Philadelphia
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

    Learn more about this trial

    Vitamin D3 for the Treatment of Low Vitamin D in Cystic Fibrosis

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