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Vitamin D Dose Finding Study

Primary Purpose

HIV Infections, AIDS

Status
Completed
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Cholecalciferol (Vit D3)
Sponsored by
Children's Hospital of Philadelphia
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for HIV Infections focused on measuring Human Immunodeficiency Virus, Acquired Immune Deficiency Syndrome, Vitamin D, HIV, Complementary therapies

Eligibility Criteria

5 Years - 24 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  1. HIV seropositive diagnosed with standard techniques
  2. Age for perinatally-acquired HIV/AIDS Group (PA subjects): 5.0 to 24.9 y
  3. Age for non-perinatally-acquired HIV/AIDS Group (non-PA subjects): 15.0 to 24.9 y
  4. In usual state of good health (no hospitalizations, emergency room or unscheduled acute illness visits for 2 weeks prior)
  5. Subject and/or family commitment to the 3-month study

Exclusion Criteria:

  1. Other chronic health conditions that may affect growth, dietary intake, and/or nutritional status
  2. Pregnancy
  3. Participation in another HIV intervention study with impact on 25D serum concentrations
  4. Use of vit D supplementation (subjects willing to discontinue supplementation will become eligible after a 2-month washout period)
  5. Baseline elevated serum calcium concentration
  6. Non-English speaking

Sites / Locations

  • Children's Hospital of Philadelphia

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Active Comparator

Arm Label

4000IU

7000IU

Arm Description

Subjects in this arm take a daily dose of 4000IU of Vitamin D3

Subjects in this arm of the study take a daily dose of 7000IU of Vitamin D3

Outcomes

Primary Outcome Measures

Safety
Determined by incidence of elevated serum calcium (above age specific range) associated with elevated serum 25D concentrations (>160ng/ml).
Efficacy of the Two Doses (4000 and 7000 IU/d)
Daily D3 supplementation will result in 25D >= to 32/ng/ml

Secondary Outcome Measures

Full Information

First Posted
March 23, 2010
Last Updated
August 1, 2013
Sponsor
Children's Hospital of Philadelphia
Collaborators
National Institutes of Health (NIH), National Center for Complementary and Integrative Health (NCCIH)
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1. Study Identification

Unique Protocol Identification Number
NCT01092338
Brief Title
Vitamin D Dose Finding Study
Official Title
Safe and Effective Vitamin D Supplementation in HIV
Study Type
Interventional

2. Study Status

Record Verification Date
August 2013
Overall Recruitment Status
Completed
Study Start Date
January 2010 (undefined)
Primary Completion Date
January 2011 (Actual)
Study Completion Date
January 2011 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Children's Hospital of Philadelphia
Collaborators
National Institutes of Health (NIH), National Center for Complementary and Integrative Health (NCCIH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Optimal vitamin D (vit D) concentration and metabolism are essential for normal immune function, growth, muscle, bone, and inflammatory status in children, adolescents and adults with HIV/AIDS. The impact of vit D supplementation will be evaluated for safety and efficacy using clinically important outcomes, and this will overcome the critical barrier for use of vit D supplementation in research and clinical care. Inexpensive and easy to administer, vit D supplementation may prove to be an effective and feasible treatment for symptoms and prevention of side effects for people of all ages living with HIV/AIDS in the US and around the world.
Detailed Description
The key role of vitamin D (vit D) in maintaining optimal bone health has long been recognized, but its role in modulating the innate immune response and inflammatory reaction has only recently come under active investigation. As such, vit D is an increasingly frequently chosen and prescribed high dose dietary supplement,because it is thought to improve immune and inflammatory status in healthy people of all ages, and in those with chronic diseases including HIV/AIDS. Vit D also has calciotrophic functions essential for bone health, and poor vit D status contributes to the osteopenia/osteoporosis associated with antiretroviral therapy (ART). Vit D may improve insulin/glucose/lipid metabolism, blood pressure and risk of some cancers, all of which may complicate HIV/AIDS and its treatments. Poor vit D status is common in patients with HIV/AIDS of all ages and factors such as age, skin pigment, lactose intolerance and sun exposure alter the risks for vit D deficiency. In the multicenter U.S. REACH study of adolescents (72% African American), with and without HIV, showed that 87% had low serum 25D concentrations (<15 ng/mL), compared to 34% in a recent sample of healthy African American children from Philadelphia. Young African Americans are disproportionately affected by HIV infection in the US (~ 55% among persons with HIV aged 13 to 24 years are African American), and are also at high risk for vit D deficiency. Vit D therapy has great promise to improve major medical conditions and the quality of life for our patients with HIV/AIDS, yet the potential role of vit D in the treatment of HIV/AIDS has not been formally tested. Well-designed randomized trials are urgently needed to determine vit D supplementation safety and efficacy. The investigators propose a two-phase study to establish safety and efficacy of high dose vit D supplementation in children and adults with HIV/AIDS. In Study Phase I, the safety and efficacy of two oral vit D3 doses (4000 and 7000 IU/d) are determined over 12 weeks in 44 subjects ages 5.0 to 24.9 y. The key safety measure is concurrently elevated serum calcium and 25D concentrations. Efficacy is evaluated by serum 25D concentration and cathelicidin (innate immune, antimicrobial protein) mRNA expression. Study Phase II is a 12 month, double blind, randomized, placebo controlled supplementation study (n=52). Key outcomes include safety and longterm 25D concentration within the goal range (32 to 160 ng/mL), improved cathelicidin mRNA expression, and measures of bone, muscle, inflammation, growth and body composition status, and HIV/AIDS disease severity. Based on the evidence and promise, vit D clearly deserves to be among the first nutrients evaluated in the National Center for Complimentary and Alternative Medicine (NCCAM) HIV research program.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, AIDS
Keywords
Human Immunodeficiency Virus, Acquired Immune Deficiency Syndrome, Vitamin D, HIV, Complementary therapies

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
44 (Actual)

8. Arms, Groups, and Interventions

Arm Title
4000IU
Arm Type
Active Comparator
Arm Description
Subjects in this arm take a daily dose of 4000IU of Vitamin D3
Arm Title
7000IU
Arm Type
Active Comparator
Arm Description
Subjects in this arm of the study take a daily dose of 7000IU of Vitamin D3
Intervention Type
Drug
Intervention Name(s)
Cholecalciferol (Vit D3)
Other Intervention Name(s)
Carlson D Drops: The D Drop Company, Nutraceutical Life Sciences Vitamin D3 2000 IU capsules: Vitacost, NOW Foods 5000 IU softgels: Now Health Group, Inc.
Intervention Description
To test two oral daily doses (4000 vs. 7000 IU) of cholecalciferol (D3) dietary supplement (capsules or liquid) over a 3-month period in 44 children, adolescents and adults with HIV/AIDS.
Primary Outcome Measure Information:
Title
Safety
Description
Determined by incidence of elevated serum calcium (above age specific range) associated with elevated serum 25D concentrations (>160ng/ml).
Time Frame
12 weeks
Title
Efficacy of the Two Doses (4000 and 7000 IU/d)
Description
Daily D3 supplementation will result in 25D >= to 32/ng/ml
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
24 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HIV seropositive diagnosed with standard techniques Age for perinatally-acquired HIV/AIDS Group (PA subjects): 5.0 to 24.9 y Age for non-perinatally-acquired HIV/AIDS Group (non-PA subjects): 15.0 to 24.9 y In usual state of good health (no hospitalizations, emergency room or unscheduled acute illness visits for 2 weeks prior) Subject and/or family commitment to the 3-month study Exclusion Criteria: Other chronic health conditions that may affect growth, dietary intake, and/or nutritional status Pregnancy Participation in another HIV intervention study with impact on 25D serum concentrations Use of vit D supplementation (subjects willing to discontinue supplementation will become eligible after a 2-month washout period) Baseline elevated serum calcium concentration Non-English speaking
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Virginia Stallings, MD
Organizational Affiliation
Children's Hospital of Philadelphia
Official's Role
Principal Investigator
Facility Information:
Facility Name
Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
23059649
Citation
Groleau V, Herold RA, Schall JI, Wagner JL, Dougherty KA, Zemel BS, Rutstein RM, Stallings VA. Blood lead concentration is not altered by high-dose vitamin D supplementation in children and young adults with HIV. J Pediatr Gastroenterol Nutr. 2013 Mar;56(3):316-9. doi: 10.1097/MPG.0b013e3182758c4a.
Results Reference
result
PubMed Identifier
26625449
Citation
Dougherty KA, Schall JI, Zemel BS, Tuluc F, Hou X, Rutstein RM, Stallings VA. Safety and Efficacy of High-Dose Daily Vitamin D3 Supplementation in Children and Young Adults Infected With Human Immunodeficiency Virus. J Pediatric Infect Dis Soc. 2014 Dec;3(4):294-303. doi: 10.1093/jpids/piu012. Epub 2014 Mar 27.
Results Reference
derived

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Vitamin D Dose Finding Study

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