Multi-center Clinical Evaluation of Three Reagent Kits Based on Interferon-gama Release Assay for the Rapid Diagnosis of Tuberculosis

Multi-center Clinical Evaluation of Three Reagent Kits Based on Interferon-gama Release Assay for th

Status

Active, not recruiting

Phases

Phase 4

Study type

Observational

Source

ChiCTR

Registry ID

ChiCTR-DDT-14005237

Enrollment

Unknown

Registered

2014-08-09

Start date

2012-09-01

Completion date

Unknown

Last updated

2017-04-18

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

Conditions

None listed

Interventions

Gold Standard:

Index test:

Eligibility

Age

2 Years to 89 Years

Inclusion criteria

Inclusion criteria: patients with pulmonary TB and extra-pulmonary TB, patients with pulmonary disease but not TB, health peopleall of the participants were negative for human immunodeficiency virus (HIV)/acquired immunodeficiency syndrome (AIDS) diagnosed with China national" Diagnostic criteria for HIV/AIDS".

Exclusion criteria

Exclusion criteria: Patients disobidence, HIV positive, without a clear test result of ?-release assay.

Design outcomes

Primary

Measure	Time frame
positive rate;negative rate;	—

Countries

China

Contacts

Public ContactKanglin Wan

wankanglin@icdc.cn+86 010-58900779

Outcome results