QuantiFERON Change During Anti-tuberculosis Medication
Completed
- Conditions
- TuberculosisInterferon-gamma Release Assay
- Registration Number
- NCT01038830
- Lead Sponsor
- Armed Forces Capital Hospital, Republic of Korea
- Brief Summary
The aim of this study is to evaluate the change of QuantiFERON-TB gold in tube assay (QFT) during the treatment of active tuberculosis.
- Detailed Description
Patients with active pulmonary tuberculosis are enrolled and, QFTs are performed for each subjects before treatment and 1, 3, 6 months after treatment. Investigators check the level of interferon-gamma, and reversion and conversion of this test.
Recruitment & Eligibility
- Status
- COMPLETED
- Sex
- All
- Target Recruitment
- 50
Inclusion Criteria
- All subjects with active tuberculosis
Exclusion Criteria
- Subjects who cannot complete study
- Subjects who have taken anti-tuberculosis medication for more than a month before visit of our hospital
Study & Design
- Study Type
- OBSERVATIONAL
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method
Trial Locations
- Locations (1)
Armed Forces Capital Hospital
🇰🇷Seongnam, Gyeonggi-do, Korea, Republic of