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

Sponsor
Harvard School of Public Health (HSPH) (Other)
Overall Status
Completed
CT.gov ID
NCT01657656
Collaborator
(none)
350
1
2
21
16.7

Study Details

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

Condition or Disease Intervention/Treatment Phase
  • Dietary Supplement: Vitamin D
N/A

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.

Study Design

Study Type:
Interventional
Anticipated Enrollment :
350 participants
Allocation:
Randomized
Intervention Model:
Parallel Assignment
Masking:
Double (Participant, Investigator)
Primary Purpose:
Treatment
Official Title:
Vitamin D Supplementations as Adjunct to Anti-Tuberculosis Drugs in Mongolia
Study Start Date :
Oct 1, 2012
Actual Primary Completion Date :
May 1, 2014
Actual Study Completion Date :
Jul 1, 2014

Arms and Interventions

Arm Intervention/Treatment
Experimental: Vitamin D group

Vitamin D supplement by Tishcon

Dietary Supplement: Vitamin D

Placebo Comparator: Control group

Identically appearing capsules

Dietary Supplement: Vitamin D

Outcome Measures

Primary Outcome Measures

  1. The primary endpoint will be time to sputum culture conversion from positive to negative. [Eight weeks]

Eligibility Criteria

Criteria

Ages Eligible for Study:
18 Years to 80 Years
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
No
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

Contacts and Locations

Locations

Site City State Country Postal Code
1 National Center for Communicable Dieases Ulaanbaatar Mongolia

Sponsors and Collaborators

  • Harvard School of Public Health (HSPH)

Investigators

None specified.

Study Documents (Full-Text)

None provided.

More Information

Publications

None provided.
Responsible Party:
Ganmaa Davaasambuu, Assistant Professor, Harvard School of Public Health (HSPH)
ClinicalTrials.gov Identifier:
NCT01657656
Other Study ID Numbers:
  • R00HL089710
First Posted:
Aug 6, 2012
Last Update Posted:
Jul 30, 2014
Last Verified:
Jul 1, 2014
Additional relevant MeSH terms:

Study Results

No Results Posted as of Jul 30, 2014