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Vitamin D Supplementations as Adjunct to Anti-Tuberculosis Drugs in Mongolia

Primary Purpose

Vitamin D Supplements, Tuberculosis, Sputum

Status
Completed
Phase
Not Applicable
Locations
Mongolia
Study Type
Interventional
Intervention
Vitamin D
Sponsored by
Harvard School of Public Health (HSPH)
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Vitamin D Supplements

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Sputum positive TB patients

Exclusion Criteria:

  • We will exclude those with abnormal LFTs at baseline (2.5 times upper limit of normal), as they will be at higher risk of developing drug-induced hepatitis

Sites / Locations

  • National Center for Communicable Dieases

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Placebo Comparator

Arm Label

Vitamin D group

Control group

Arm Description

Vitamin D supplement by Tishcon

Identically appearing capsules

Outcomes

Primary Outcome Measures

The primary endpoint will be time to sputum culture conversion from positive to negative.

Secondary Outcome Measures

Full Information

First Posted
August 2, 2012
Last Updated
July 29, 2014
Sponsor
Harvard School of Public Health (HSPH)
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1. Study Identification

Unique Protocol Identification Number
NCT01657656
Brief Title
Vitamin D Supplementations as Adjunct to Anti-Tuberculosis Drugs in Mongolia
Official Title
Vitamin D Supplementations as Adjunct to Anti-Tuberculosis Drugs in Mongolia
Study Type
Interventional

2. Study Status

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

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Harvard School of Public Health (HSPH)

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Hypothesis That improving vitamin D status among TB patients will speed the pace of bacteriological cure, and will enhance immune responses to TB infection
Detailed Description
Tuberculosis (TB) will be the world's largest single cause of death from infection for the 30-year period between 1990 and 2020. More than 95% of TB cases, and deaths due to TB, occur in developing countries. Mongolia is one of the countries with the highest tuberculosis burdens in the Western Pacific region. In addition, vitamin D deficiency is endemic in Mongolia. We propose to determine the efficacy of vitamin D supplements, as an adjunct to multidrug therapy, in enhancing the anti-microbial immune response to TB, a finding that could lead to the development of shorter drug regimens, and thus more efficient and effective TB treatment protocols. We propose to conduct a double blind, placebo controlled, randomized clinical trial to test the effect of a daily vitamin D supplementation on the ability of subjects to control TB infection. The Primary Endpoint: The primary endpoint will be: time to sputum culture conversion from positive to negative. The number of days to sputum conversion will be measured, in both the intervention and control groups, starting on the date that treatment is begun. Sputum samples will be collected and cultured every two weeks thereafter. The date of conversion from positive to negative, for each subject, will be the date halfway between the date of the last culture-positive sputum and the first culture-negative one. Secondary Endpoints: Bacteriologic secondary endpoints, cell-mediated immune function endpoints and BMI.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Vitamin D Supplements, Tuberculosis, Sputum, Cytokines, Immunity

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
350 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Vitamin D group
Arm Type
Experimental
Arm Description
Vitamin D supplement by Tishcon
Arm Title
Control group
Arm Type
Placebo Comparator
Arm Description
Identically appearing capsules
Intervention Type
Dietary Supplement
Intervention Name(s)
Vitamin D
Primary Outcome Measure Information:
Title
The primary endpoint will be time to sputum culture conversion from positive to negative.
Time Frame
Eight weeks

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Sputum positive TB patients Exclusion Criteria: We will exclude those with abnormal LFTs at baseline (2.5 times upper limit of normal), as they will be at higher risk of developing drug-induced hepatitis
Facility Information:
Facility Name
National Center for Communicable Dieases
City
Ulaanbaatar
Country
Mongolia

12. IPD Sharing Statement

Citations:
PubMed Identifier
28692301
Citation
Ganmaa D, Munkhzul B, Fawzi W, Spiegelman D, Willett WC, Bayasgalan P, Baasansuren E, Buyankhishig B, Oyun-Erdene S, Jolliffe DA, Xenakis T, Bromage S, Bloom BR, Martineau AR. High-Dose Vitamin D3 during Tuberculosis Treatment in Mongolia. A Randomized Controlled Trial. Am J Respir Crit Care Med. 2017 Sep 1;196(5):628-637. doi: 10.1164/rccm.201705-0936OC.
Results Reference
derived

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Vitamin D Supplementations as Adjunct to Anti-Tuberculosis Drugs in Mongolia

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