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Latent Tuberculosis Infection in Bone Marrow Transplant Recipients

A

Asan Medical Center

Status

Completed

Conditions

Tuberculosis

Study type

Observational

Funder types

Other

Identifiers

NCT01021124
2009-0077

Details and patient eligibility

About

The aim of this study is to estimate the usefulness of a T cell-based assay (i.e. Quantiferon-Gold In-Tube assay) for diagnosis of latent tuberculosis infection (LTBI) in bone marrow transplant recipients. For this purpose, the investigators enrolled bone marrow transplant recipients and observed the developement of tuberculosis after the transplantation.

Full description

All adult bone marrow transplant recipients admitted to Asan Medical Center will be enrolled.

Quantiferon-Gold In-Tube assay will be performed.

Isoniazid prophylaxis will be given only to patients with clinical risk factors (i.e. recent contact with active pulmonary TB patient or inadequate treatment history with abnormal CXR). However, isoniazid prophylaxis will be not given based on positive TST or positive Quantiferon-Gold In-Tube assay.

Enrollment

409 patients

Sex

All

Ages

16+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Age 16 or more
  • Bone marrow transplant recipients

Exclusion criteria

  • Recent contact of patients with active pulmonary tuberculosis
  • Suspected active tuberculosis

Trial design

409 participants in 1 patient group

QFT (+) vs QFT (-)

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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