The Safety, Completion Rate and Prevention Effect by Rifamycin-containing Regimens for Latent Tuberculosis Infection in Patients With Kidney Transplantation: a Prospective Intervention Pilot Study

Recruiting Phase 4 Interventional Study
Pulmonology
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Prior Safety Data This treatment has already been tested in at least one earlier human trial.
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At a Glance
Age
20 and older
Sex
Any
Trial phase
Phase 4
Study type
Interventional
Purpose
Treatment
Participants needed
500 (estimated)
Sponsor
National Taiwan University Hospital · Other
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About This Trial
Tuberculosis (TB) remains the leading infectious disease worldwide and kidney transplant recipients (KTR) is high risk population needing prevention from reactivation, which cause high mortality. In fact, its latent tuberculosis infection (LTBI) is increasing after transplantation and has been identified as a risk factor for TB. However, the suitable regimen for LTBI treatment in KTRs remains uncl…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. Received kidney transplant, and 2. Will receive interferon-gamma release assay (IGRA) for LTBI, and 3. If IGRA was positive, participants agree to receive LTBI treatment Exclusion Criteria: 1. Age \< 20 years old 2. pregnancy 3. Suspicious active tuberculosis
Contacts

Chin-Chung Shu

+886-2312-3456

ccshu@ntu.edu.tw

CONTACT