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Nutrition, Immunology and Epidemiology of Tuberculosis

Primary Purpose

Tuberculosis

Status
Completed
Phase
Phase 3
Locations
United States
Study Type
Interventional
Intervention
Multivitamins
Placebo
Sponsored by
Harvard School of Public Health (HSPH)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Tuberculosis focused on measuring Tuberculosis, HIV, Tanzania, multivitamins

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Men and women, age 18 to 60 years inclusive At least two positive sputum smears for tuberculosis Intention to stay in Dar-es-Salaam for at least 2 years after the start of TB therapy Subjects who grant informed consent to participation Exclusion Criteria: Karnofsky score < 40% Hemoglobin < 8.5 g/dl Having had treatment for TB exceeding 4 weeks in the last 5 years Pregnant women

Sites / Locations

  • Harvard School of Public Health

Arms of the Study

Arm 1

Arm 2

Arm Type

Placebo Comparator

Experimental

Arm Label

Placebo

Multivitamins

Arm Description

Placebo

5000 IU of retinol, 20 mg of B1, 20 mg of B2, 25 mg of B6, 100 mg of niacin, 50 mcg of B12, 500 of C, 200 mg of E, 0.8 mg of folic acid, and 100 mcg of selenium

Outcomes

Primary Outcome Measures

To determine the efficacy of micronutrient supplements on sputum conversion, survival, and TB relapse and reinfection.

Secondary Outcome Measures

To examine the effect of micronutrient supplements on HIV viral load, CD4 counts, body weight and immunological parameters.

Full Information

First Posted
September 12, 2005
Last Updated
November 9, 2010
Sponsor
Harvard School of Public Health (HSPH)
Collaborators
Muhimbili University of Health and Allied Sciences
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1. Study Identification

Unique Protocol Identification Number
NCT00197704
Brief Title
Nutrition, Immunology and Epidemiology of Tuberculosis
Official Title
Nutrition, Immunology and Epidemiology of Tuberculosis
Study Type
Interventional

2. Study Status

Record Verification Date
November 2010
Overall Recruitment Status
Completed
Study Start Date
March 2000 (undefined)
Primary Completion Date
May 2004 (Actual)
Study Completion Date
May 2004 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
Harvard School of Public Health (HSPH)
Collaborators
Muhimbili University of Health and Allied Sciences

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The purpose of this study is to determine the efficacy of micronutrient supplementation among patients with active tuberculosis, half of who are co-infected with HIV-1
Detailed Description
Tuberculosis (TB) remains the single most common infectious disease cause of mortality. We propose to examine the inter- relationships of nutrition, immunology, and epidemiology with respect to TB in Tanzania. Given that TB is so much linked with HIV immunologically, clinically, and epidemiologically, it is essential to examine how these relationships are modified by HIV infection. Published animal and human studies suggest that vitamin deficiency is associated with poor immune response in TB. By modulating immune function, nutritional supplements may be a useful adjunct to anti-TB drugs, and could lead to the development of shorter drug regimens. All patients will receive standard anti-TB therapy. Follow-up visits will occur every two weeks for the first 2 months and monthly thereafter till the end of the study.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tuberculosis
Keywords
Tuberculosis, HIV, Tanzania, multivitamins

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Placebo
Arm Type
Placebo Comparator
Arm Description
Placebo
Arm Title
Multivitamins
Arm Type
Experimental
Arm Description
5000 IU of retinol, 20 mg of B1, 20 mg of B2, 25 mg of B6, 100 mg of niacin, 50 mcg of B12, 500 of C, 200 mg of E, 0.8 mg of folic acid, and 100 mcg of selenium
Intervention Type
Dietary Supplement
Intervention Name(s)
Multivitamins
Intervention Description
5000 IU of retinol, 20 mg of B1, 20 mg of B2, 25 mg of B6, 100 mg of niacin, 50 mcg of B12, 500 of C, 200 mg of E, 0.8 mg of folic acid, and 100 mcg of selenium taken orally on a daily basis from the start of TB therapy through 8 months of anti-TB therapy
Intervention Type
Other
Intervention Name(s)
Placebo
Intervention Description
Placebo pill taken orally on a daily basis from the start of TB therapy through 8 months of anti-TB therapy
Primary Outcome Measure Information:
Title
To determine the efficacy of micronutrient supplements on sputum conversion, survival, and TB relapse and reinfection.
Time Frame
Sputum and culture negativity: 1 month and 2 months; Survival: 8 months and 24 months; TB relapse and reinfection: throughout follow-up.
Secondary Outcome Measure Information:
Title
To examine the effect of micronutrient supplements on HIV viral load, CD4 counts, body weight and immunological parameters.
Time Frame
Rate of change of HIV viral load in HIV positive patients: 2, 5, 8, and 20 months; Absolute change in CD4 counts: 2, 5, 8, and 20 months; Weight change from baseline: 2, 8, and 20 months; Immunological parameters: 2, 8, and 20 months.

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Men and women, age 18 to 60 years inclusive At least two positive sputum smears for tuberculosis Intention to stay in Dar-es-Salaam for at least 2 years after the start of TB therapy Subjects who grant informed consent to participation Exclusion Criteria: Karnofsky score < 40% Hemoglobin < 8.5 g/dl Having had treatment for TB exceeding 4 weeks in the last 5 years Pregnant women
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Wafaie W Fawzi, MD,DrPh
Organizational Affiliation
Harvard School of Public Health (HSPH)
Official's Role
Principal Investigator
Facility Information:
Facility Name
Harvard School of Public Health
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02115
Country
United States

12. IPD Sharing Statement

Citations:
PubMed Identifier
18471061
Citation
Villamor E, Mugusi F, Urassa W, Bosch RJ, Saathoff E, Matsumoto K, Meydani SN, Fawzi WW. A trial of the effect of micronutrient supplementation on treatment outcome, T cell counts, morbidity, and mortality in adults with pulmonary tuberculosis. J Infect Dis. 2008 Jun 1;197(11):1499-505. doi: 10.1086/587846.
Results Reference
result
PubMed Identifier
24247327
Citation
Mehta S, Mugusi FM, Bosch RJ, Aboud S, Urassa W, Villamor E, Fawzi WW. Vitamin D status and TB treatment outcomes in adult patients in Tanzania: a cohort study. BMJ Open. 2013 Nov 18;3(11):e003703. doi: 10.1136/bmjopen-2013-003703.
Results Reference
derived

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Nutrition, Immunology and Epidemiology of Tuberculosis

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