search
Back to results

Botswana Vitamin D Supplementation Study in HIV/AIDS

Primary Purpose

HIV

Status
Completed
Phase
Phase 3
Locations
Botswana
Study Type
Interventional
Intervention
4000 IU/d D3 over 12 weeks
7000 IU/d D3 over 12 weeks
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 focused on measuring Vitamin D

Eligibility Criteria

5 Years - 51 Years (Child, Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • HIV infection
  • Ages 5.0 to 50.9 y
  • In usual state of good health
  • Subject and/or family commitment to the 12-week study

Exclusion Criteria:

  • Other chronic health conditions unrelated to HIV/AIDS that may affect nutritional status
  • Use of vit D supplementation above 400 IU/d

Sites / Locations

  • Princess Marina Hospital

Arms of the Study

Arm 1

Arm 2

Arm Type

Active Comparator

Experimental

Arm Label

4000 IU/d of D3 by mouth for 12 weeks

7000IU/d of D3 by mouth for 12 weeks

Arm Description

4000 IU/d of D3 by mouth for 12 weeks

7000IU/d of D3 by mouth for 12 weeks

Outcomes

Primary Outcome Measures

To test the efficacy of two oral doses (4000 vs 7000 IU/d) of cholecalciferol (D3) in 60 children and adults (5.0 to 50.9 y) with HIV/AIDS to replete vit D status (achieving a minimum serum 25D concentration of 32 ng/mL).
To test two oral doses (4000 vs 7000 IU/d) of cholecalciferol (D3) over a 12-week period in 60 children and adults (5.0 to 50.9 y) with HIV/AIDS to assess 25D concentrations and efficacy to replete vit D status as determined by achieving a minimum serum 25D concentration of 32 ng/mL.
To test the safety of two oral doses (4000 vs 7000 IU/d) of cholecalciferol (D3) over a 12-week period in 60 children and adults (5.0 to 50.9 y) with HIV/AIDS as determined by serum calcium.
To test two oral doses (4000 vs 7000 IU/d) of cholecalciferol (D3) over a 12-week period in 60 children and adults (5.0 to 50.9 y) with HIV/AIDS to assess safety as determined by serum calcium.

Secondary Outcome Measures

Full Information

First Posted
July 11, 2014
Last Updated
July 14, 2014
Sponsor
Children's Hospital of Philadelphia
search

1. Study Identification

Unique Protocol Identification Number
NCT02189902
Brief Title
Botswana Vitamin D Supplementation Study in HIV/AIDS
Official Title
Botswana Vitamin D Supplementation Study in HIV/AIDS
Study Type
Interventional

2. Study Status

Record Verification Date
July 2014
Overall Recruitment Status
Completed
Study Start Date
January 2012 (undefined)
Primary Completion Date
July 2012 (Actual)
Study Completion Date
July 2012 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Children's Hospital of Philadelphia

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The goal is to determine the vit D supplementation dose that safely results in optimal serum vitamin D (25D) concentrations in HIV-infected children and adults living in Botswana. To do this the investigators will test two oral daily doses (4000 vs. 7000 IU) of cholecalciferol (D3) dietary supplement over a 12-week period in 60 children and adults with HIV/AIDS living in Botswana (5.0 to 50.9 yrs), to assess safety as determined by serum calcium and 25D concentrations and efficacy to replete vit D status as determined by achieving a minimum serum 25D concentration of 32 ng/mL (80 nmol/L).
Detailed Description
Many people living with HIV/AIDS in African countries are vit D deficient or insufficient. Vit D deficiency in HIV/AIDS may be due to low dietary vit D intake, increased requirements, malabsorption, specific drug therapies (antiretrovirals, in particular), reduced outdoor physical activity, reduced vit D synthesis from UV light exposure in dark skin pigmented individuals, or unknown HIV-associated factors. Vit D deficiency likely contributes to abnormal immune status and increased inflammatory state, and to poor growth, bone, and muscle function, and may contribute to risk for tuberculosis (TB) infection. The goal is to determine the vit D supplementation dose that safely results in optimal serum 25D concentrations in HIV-infected children and adults living in Botswana. To do this the investigators will test two oral daily doses (4000 vs. 7000 IU) of cholecalciferol (D3) dietary supplement over a 12-week period in 60 children and adults with HIV/AIDS living in Botswana (5.0 to 50.9 yrs), to assess safety as determined by serum calcium and 25D concentrations and efficacy to replete vit D status as determined by achieving a minimum serum 25D concentration of 32 ng/mL (80 nmol/L).

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV
Keywords
Vitamin D

7. Study Design

Primary Purpose
Treatment
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
60 (Actual)

8. Arms, Groups, and Interventions

Arm Title
4000 IU/d of D3 by mouth for 12 weeks
Arm Type
Active Comparator
Arm Description
4000 IU/d of D3 by mouth for 12 weeks
Arm Title
7000IU/d of D3 by mouth for 12 weeks
Arm Type
Experimental
Arm Description
7000IU/d of D3 by mouth for 12 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
4000 IU/d D3 over 12 weeks
Intervention Type
Dietary Supplement
Intervention Name(s)
7000 IU/d D3 over 12 weeks
Primary Outcome Measure Information:
Title
To test the efficacy of two oral doses (4000 vs 7000 IU/d) of cholecalciferol (D3) in 60 children and adults (5.0 to 50.9 y) with HIV/AIDS to replete vit D status (achieving a minimum serum 25D concentration of 32 ng/mL).
Description
To test two oral doses (4000 vs 7000 IU/d) of cholecalciferol (D3) over a 12-week period in 60 children and adults (5.0 to 50.9 y) with HIV/AIDS to assess 25D concentrations and efficacy to replete vit D status as determined by achieving a minimum serum 25D concentration of 32 ng/mL.
Time Frame
12 weeks
Title
To test the safety of two oral doses (4000 vs 7000 IU/d) of cholecalciferol (D3) over a 12-week period in 60 children and adults (5.0 to 50.9 y) with HIV/AIDS as determined by serum calcium.
Description
To test two oral doses (4000 vs 7000 IU/d) of cholecalciferol (D3) over a 12-week period in 60 children and adults (5.0 to 50.9 y) with HIV/AIDS to assess safety as determined by serum calcium.
Time Frame
12 weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
5 Years
Maximum Age & Unit of Time
51 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: HIV infection Ages 5.0 to 50.9 y In usual state of good health Subject and/or family commitment to the 12-week study Exclusion Criteria: Other chronic health conditions unrelated to HIV/AIDS that may affect nutritional status Use of vit D supplementation above 400 IU/d
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
Princess Marina Hospital
City
Gaborone
ZIP/Postal Code
0000
Country
Botswana

12. IPD Sharing Statement

Citations:
PubMed Identifier
25706751
Citation
Steenhoff AP, Schall JI, Samuel J, Seme B, Marape M, Ratshaa B, Goercke I, Tolle M, Nnyepi MS, Mazhani L, Zemel BS, Rutstein RM, Stallings VA. Vitamin D(3)supplementation in Batswana children and adults with HIV: a pilot double blind randomized controlled trial. PLoS One. 2015 Feb 23;10(2):e0117123. doi: 10.1371/journal.pone.0117123. eCollection 2015.
Results Reference
derived

Learn more about this trial

Botswana Vitamin D Supplementation Study in HIV/AIDS

We'll reach out to this number within 24 hrs