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Completed

NCT Number: NCT00677339

L-arginine and Vitamin D Adjunctive Therapy in Pulmonary Tuberculosis (TB)

The purpose of this study is to determine whether adjunctive L-arginine and vitamin D can improve response to standard short course TB therapy in people with newly diagnosed pulmonary TB.

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Key information

Age range

15 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 3

Primary location

Timika Tuberculosis Clinic and Community Hospital

Timika, Papua Province, Indonesia

About this study

The two major pathways proposed to mediate macrophage mycobacterial killing in humans are the arginine-nitric oxide and Vitamin D-1,25 dihydroxyvitamin D pathways. Our aim is to determine if the key immunomodulatory agents L-arginine and vitamin D can improve the rapidity and magnitude of the microbiological and clinical response in pulmonary TB. We will test the following hypotheses in newly-diagnosed TB patients in Timika, Papua, Indonesia:

Our specific aims are to:

  • Determine whether supplementation with L-arginine and/or vitamin D is safe, and results in more rapid improvement in clinical, mycobacterial, immunological, radiological, physiological and functional measures of treatment outcome. We will randomise patients with pulmonary TB to receive, in addition to standard TB therapy, adjunctive arginine, vitamin D and / or placebo in a randomised, double-blind factorial 2x2 design. We will relate serial measurements of plasma concentrations of L-arginine and vitamin D, and immunological responses (pulmonary NO production, T cell function and phenotype) to measures of treatment outcome [mycobacterial (sputum smear clearance and culture conversion), physiological (spirometry), clinical (symptoms and weight), radiological (chest Xray) and functional (six-minute walk test, modified St George Respiratory Questionnaire)].
  • Determine whether pulmonary production of NO is inversely related to disease severity at presentation. Baseline and serial measures of NO production will be related to disease severity and the magnitude and rapidity of clinical response

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Adults >15 years with sputum smear positive pulmonary TB
  • New cases only
  • Agree to continue treatment in Timika for the full six month course of treatment -Not pregnant
  • Consent to enroll in the study.

Exclusion criteria

  • hypercalcaemia (ionized calcium >1.32 mmol/L) identified at baseline
  • taking arginine or vitamin D

Treatment and study plan

L-arginine

Drug

L-arginine 6g orally daily

Other names: Argimax

Vitamin D

Drug

Cholecalciferol 50000 IU once monthly orally

Other names: Calciferol Strong

Placebo L-arginine

Drug

placebo L-arginine once daily

Placebo Vitamin D

Drug

placebo vitamin D orally once monthly

Primary outcomes

  1. Proportion of pulmonary TB patients who are culture negative at 1 month

    Time frame: 1 month

  2. Difference in improvement in composite clinical endpoint comprising weight, cough clearance and FEV1 at 2 months.

    Time frame: 2 months

Secondary outcomes

  1. Change in plasma L-arginine concentration

    Time frame: week 0, 2, 4, 8, 24

  2. Change in plasma 25(OH)D3 concentration

    Time frame: week 0, 2, 4, 8, 24

  3. Death, clinical failure and default independently, and 'death or clinical failure or default'.

    Time frame: week 24

  4. Hypercalcaemia

    Time frame: week 0, 2, 4, 8, 24

  5. Gastrointestinal side effects

    Time frame: weekly to week 8 then at week 24

  6. Sputum smear conversion time

    Time frame: weekly to week 8 then at week 24

  7. Radiological improvement (percentage lung involvement on CXR at 2 months).

    Time frame: week 0, 2, 4, 8, 24

  8. Cough clearance

    Time frame: weekly to week 8 then at week 24

  9. Difference in improvement in percent predicted FEV1 at 2 and 6 months.

    Time frame: weeks 0, 4, 8, 24

  10. Weight gain

    Time frame: weekly to week 8 then at week 24

  11. Immunological improvement (exhaled NO)

    Time frame: week 0, 2, 4, 8, 24

  12. Immunological improvement (T cell CD3ζ expression and T cell function)

    Time frame: week 0, 2, 4, 24

  13. Functional improvement measured using six minute walk test

    Time frame: week 0, 4, 8, 24

  14. Quality of life assessment using modified St George Respiratory Questionnaire.

    Time frame: weeks 0, 4, 8, 24

  15. Primary end points stratified by HIV status.

    Time frame: weekly to week 8 then at week 24

  16. Primary end points stratified by baseline vitamin D and L-arginine status.

    Time frame: weekly to week 8 then week 24

  17. Primary end points stratified by ethnicity (Papuan and non-Papuan patients).

    Time frame: weekly to week 8 then week 24

Sponsors and collaborators

Lead sponsor

Menzies School of Health Research

Other

Collaborators

  • Australian National University
  • National Institute of Health Research and Development, Ministry of Health Republic of Indonesia

Registry information

Official study title

Phase 3 Trial of Oral L-arginine and / or Vitamin D as Adjunctive Therapies in Pulmonary Tuberculosis in Papua Province, Indonesia.

Acronym: AVDAPT

Important dates

Study start
2008
Primary completion
2010
Study completion
2010
First posted
May 14, 2008
Registry last updated
Jan 18, 2012

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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