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

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

Status
Completed
Phases
Phase 3
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00677339
Acronym
AVDAPT
Enrollment
200
Registered
2008-05-14
Start date
2008-06-30
Completion date
2010-05-31
Last updated
2012-01-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Smear Positive Pulmonary Tuberculosis

Keywords

Tuberculosis, Adjunctive therapy, L-arginine, Nitric oxide, Vitamin D

Brief summary

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.

Detailed description

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: 1. 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 \[mycobacterial (sputum smear clearance and culture conversion), physiological (spirometry), clinical (symptoms and weight), radiological (chest Xray) and functional (six-minute walk test, modified St George Respiratory Questionnaire)\]. 2. 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

Interventions

DRUGL-arginine

L-arginine 6g orally daily

DRUGVitamin D

Cholecalciferol 50000 IU once monthly orally

DRUGPlacebo L-arginine

placebo L-arginine once daily

DRUGPlacebo Vitamin D

placebo vitamin D orally once monthly

Sponsors

National Institute of Health Research and Development, Ministry of Health Republic of Indonesia
CollaboratorOTHER
Australian National University
CollaboratorOTHER
Menzies School of Health Research
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
FACTORIAL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)

Eligibility

Sex/Gender
ALL
Age
15 Years to No maximum
Healthy volunteers
No

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

Design outcomes

Primary

MeasureTime frame
Proportion of pulmonary TB patients who are culture negative at 1 month1 month
Difference in improvement in composite clinical endpoint comprising weight, cough clearance and FEV1 at 2 months.2 months

Secondary

MeasureTime frame
Death, clinical failure and default independently, and 'death or clinical failure or default'.week 24
Hypercalcaemiaweek 0, 2, 4, 8, 24
Gastrointestinal side effectsweekly to week 8 then at week 24
Sputum smear conversion timeweekly to week 8 then at week 24
Radiological improvement (percentage lung involvement on CXR at 2 months).week 0, 2, 4, 8, 24
Cough clearanceweekly to week 8 then at week 24
Difference in improvement in percent predicted FEV1 at 2 and 6 months.weeks 0, 4, 8, 24
Change in plasma L-arginine concentrationweek 0, 2, 4, 8, 24
Immunological improvement (exhaled NO)week 0, 2, 4, 8, 24
Immunological improvement (T cell CD3ζ expression and T cell function)week 0, 2, 4, 24
Functional improvement measured using six minute walk testweek 0, 4, 8, 24
Quality of life assessment using modified St George Respiratory Questionnaire.weeks 0, 4, 8, 24
Primary end points stratified by HIV status.weekly to week 8 then at week 24
Primary end points stratified by baseline vitamin D and L-arginine status.weekly to week 8 then week 24
Primary end points stratified by ethnicity (Papuan and non-Papuan patients).weekly to week 8 then week 24
Weight gainweekly to week 8 then at week 24
Change in plasma 25(OH)D3 concentrationweek 0, 2, 4, 8, 24

Countries

Indonesia

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 23, 2026