The Effects of Nutritional Supplementation and Drug Abuse on HIV
Primary Purpose
HIV Infections, Substance-Related Disorders
Status
Completed
Phase
Not Applicable
Locations
Botswana
Study Type
Interventional
Intervention
Multivitamins
Selenium
Placebo
Sponsored by
About this trial
This is an interventional treatment trial for HIV Infections focused on measuring Treatment Naive, Multivitamins, Selenium, Supplementation, HIV Disease Progression
Eligibility Criteria
Inclusion Criteria: HIV infected CD4 count greater than 350 cells/mm3 Identified from the Infectious Disease Care Clinic Body mass index greater than 18 for women and greater than 18.5 for men Exclusion Criteria: Current AIDS-defining condition Currently participating in another clinical trial Pregnant or intends to become pregnant during the study
Sites / Locations
- Princess Marina Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Arm Type
Placebo Comparator
Experimental
Experimental
Experimental
Arm Label
1
2
3
4
Arm Description
Multivitamins
Multivitamins with Selenium
Selenium
Outcomes
Primary Outcome Measures
HIV Disease Progression
Secondary Outcome Measures
Morbidity
Full Information
NCT ID
NCT00149656
First Posted
September 6, 2005
Last Updated
April 26, 2013
Sponsor
Florida International University
Collaborators
National Institute on Drug Abuse (NIDA)
1. Study Identification
Unique Protocol Identification Number
NCT00149656
Brief Title
The Effects of Nutritional Supplementation and Drug Abuse on HIV
Official Title
HIV Disease, Drug Abuse, and Nutrient Therapy in Botswana
Study Type
Interventional
2. Study Status
Record Verification Date
April 2013
Overall Recruitment Status
Completed
Study Start Date
June 2003 (undefined)
Primary Completion Date
July 2010 (Actual)
Study Completion Date
April 2013 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Florida International University
Collaborators
National Institute on Drug Abuse (NIDA)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The purpose of this trial is to determine whether supplementation with multivitamins and selenium will delay disease progression in HIV infected individuals in Botswana. The study will also assess how drug abuse modifies the effect of nutritional supplementation on HIV disease progression.
Detailed Description
Botswana has the highest rates of HIV infection in the world. In addition, drug abuse has become an emerging problem in Botswana. Past research suggests that multivitamin and selenium supplementation slows the progression of HIV disease. The purpose of this trial is to evaluate the effectiveness of supplementation with multivitamins and selenium in HIV infected individuals in Botswana.
This trial will last 2 years. Participants will be randomly assigned to 4 groups: a combination of multivitamins with selenium, multivitamins alone, selenium alone, or placebo.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
HIV Infections, Substance-Related Disorders
Keywords
Treatment Naive, Multivitamins, Selenium, Supplementation, HIV Disease Progression
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Factorial Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
878 (Actual)
8. Arms, Groups, and Interventions
Arm Title
1
Arm Type
Placebo Comparator
Arm Title
2
Arm Type
Experimental
Arm Description
Multivitamins
Arm Title
3
Arm Type
Experimental
Arm Description
Multivitamins with Selenium
Arm Title
4
Arm Type
Experimental
Arm Description
Selenium
Intervention Type
Dietary Supplement
Intervention Name(s)
Multivitamins
Intervention Description
dietary supplement of multivitamins
Intervention Type
Dietary Supplement
Intervention Name(s)
Selenium
Intervention Description
dietary supplement of selenium only
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
placebo pill
Primary Outcome Measure Information:
Title
HIV Disease Progression
Time Frame
For at least 6 months
Secondary Outcome Measure Information:
Title
Morbidity
Time Frame
For at least 6 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
90 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
HIV infected
CD4 count greater than 350 cells/mm3
Identified from the Infectious Disease Care Clinic
Body mass index greater than 18 for women and greater than 18.5 for men
Exclusion Criteria:
Current AIDS-defining condition
Currently participating in another clinical trial
Pregnant or intends to become pregnant during the study
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marianna K. Baum, PhD
Organizational Affiliation
Florida International University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Princess Marina Hospital
City
Gaborone
Country
Botswana
12. IPD Sharing Statement
Learn more about this trial
The Effects of Nutritional Supplementation and Drug Abuse on HIV
We'll reach out to this number within 24 hrs