A15.9
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: Arm 1: presumptive pulmonary TB (including concurrent EPTB) consulting or referred to CERMEL tuberculosis laboratory for diagnostic TB work up (including microbiological investigations (TB-culture, TB-PCR) and lung imaging) Arm 2: healthy controls accompanying patients with presumed TB Arm 3: TB-healthcare providers at CERMEL
Exclusion criteria
Exclusion criteria: Arm 1: - No consent given - No TB work-up initiated by attending physician - Already under anti-TB treatment for >7 days Arm 2: - No consent given - TB work-up initiated by attending physician - TB diagnosed and/or under anti-TB treatment within past 6 months - Positive WHO-symptom screen for TB disease Arm 3: - does not agree with recording of interview
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| 1. non-tuberculous lung infection prevalence (mycobacterial, non-mycobacterial, fungal and parasitic) in patients with presumed TB 2. contribution of non-tuberculous infections to disease outcomes per “confirmed” or “clinical TB” or “no TB diagnosed” | — |
Secondary
| Measure | Time frame |
|---|---|
| Exploration of perspectives regarding the diagnostic process across different types of cases (clinical TB, no diagnosis made, confirmed TB) and preferences for TB diagnostic services of patients and providers | — |
Countries
Gabon
Contacts
Universitätsklinikum Tübingen, Institut für Tropenmedizin