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QuantiFERON Change During Anti-tuberculosis Medication

Completed
Conditions
Tuberculosis
Interferon-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
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

Armed Forces Capital Hospital

🇰🇷

Seongnam, Gyeonggi-do, Korea, Republic of

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