Fermented Soybean Supplementation Among Active Pulmonary Tuberculosis Patients With Standard Therapy in Indonesia (FSS)
Pulmonary Tuberculosis, Body Weight Changes, Motor Activity
About this trial
This is an interventional supportive care trial for Pulmonary Tuberculosis focused on measuring Tempeh, Body weight, Handgrip strength, 6MWT, Supplementation, Wasting
Eligibility Criteria
Inclusion Criteria:
- Newly diagnosed adult male and female TB active patients
- Having clinical evidences of active TB symptoms
- Positive or negative sputum smears
- Having positive chest X-ray that compatible with a diagnosis of tuberculosis
- No history of previous anti tuberculosis treatment
- Give a written informed consent and basic contact data
Exclusion Criteria:
- Heavy smoker (> 20 cigarettes per day)
- Pregnancy and lactation
- Extra pulmonary TB
- Known allergy to soybean
- Having clinical evidences of any underlying disease
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Active Comparator
Intervention
Control
TB standard therapy with fixed dose combination : once per day by mouth for 2 months Fixed dose combination = RHZE (150mg/75mg/400mg/275mg) R=rifampicin, H=isoniazid, Z=pyrazinamide, E=ethambutol, Patients with body weight: 30 - 37 kg = 2 tablets, 38 - 54 kg = 3 tablets, 55 - 70 kg = 4 tablets, and ≥71 kg = 5 tablets and 166.5 grams cooked fermented soybean (tempeh) daily for two months
TB standard therapy with fixed dose combination : once per day by mouth for 2 months Fixed dose combination = RHZE (150mg/75mg/400mg/275mg) R=rifampicin, H=isoniazid, Z=pyrazinamide, E=ethambutol, Patients with body weight: 30 - 37 kg = 2 tablets, 38 - 54 kg = 3 tablets, 55 - 70 kg = 4 tablets, and ≥71 kg = 5 tablets