Effects of Interferon-Gamma on Cavitary Pulmonary Tuberculosis in the Lungs
Tuberculosis, AIDS-related Complex
About this trial
This is an interventional treatment trial for Tuberculosis
Eligibility Criteria
Inclusion Criteria: Positive acid-fast bacillus (AFB) smear within 14 days prior to randomization Cluster of Differentiation 4 greater than 200 if HIV positive Ability to sign consent Bilateral, cavitary pulmonary TB Exclusion Criteria: Multidrug-resistant (MDR) TB Extrapulmonary TB HIV positive with opportunistic infection within 30 days of study entry Cancer Asthma Pregnant or lactating women Chronic heart disease Chronic liver disease Chronic renal disease Seizure disorder Bleeding or clotting disorder Diabetes mellitus
Sites / Locations
- NYU School of Medicine
- The Lung Institute at University of Cape Town
Arms of the Study
Arm 1
Arm 2
Arm 3
Placebo Comparator
Experimental
Experimental
Standard Treatment
Aerosol Interferon-gamma
Subcutaneous Interferon-Gamma
Isoniazid, Rifampin, Pyrazinamide Anti-Tuberculous Therapy
Aerosol Interferon-Gamma plus Isoniazid, Rifampin, and Pyrazinamide
Subcutaneous Interferon-Gamma plus Isoniazid, Rifampin, and Pyrazinamide