Use of a Gamma-IFN Assay in Contact Tracing for Tuberculosis in a Low-Incidence, High Immigration Area
Production of Gamma-Interferon by Circulating Lymphocytes Exposed to Antigens Specific of Mycobacterium Tuberculosis: Contribution to the Identification of Latent Tuberculosis Infection in Contact Tracing
1 other identifier
observational
295
1 country
1
Brief Summary
After exposure to an active case of tuberculosis (TB), close contacts may be infected. They are then considered as having latent tuberculosis infection (LTBI). Detecting LTBI is the main goal of contact tracing procedures after exposure to TB. Until recently, the only test available for detecting LTBI was the tuberculin skin test (TST). More recent tests are now available (Interferon-gamma release assays: IGRA), which are more specific and sensitive than the TST. This study compares the TST and an IGRA in the routine activity of contact tracing in our area.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Oct 2004
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
October 1, 2004
CompletedStudy Completion
Last participant's last visit for all outcomes
January 1, 2006
CompletedFirst Submitted
Initial submission to the registry
November 13, 2007
CompletedFirst Posted
Study publicly available on registry
November 14, 2007
CompletedNovember 14, 2007
November 1, 2007
November 13, 2007
November 13, 2007
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Correlation between results of TST and IGRA tests and exposure scores
2 months after exposure
Eligibility Criteria
All subjects screened after exposure to a case of active and contagious tuberculosis in the Geneva area
You may qualify if:
- Exposure to a case of contagious TB
- Willingness to participate in study
You may not qualify if:
- Known HIV infection
- Known previous TB or treatment for LTBI
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- University Hospital, Genevalead
- Ligue Pulmonaire Genevoisecollaborator
Study Sites (1)
Centre antituberculeux; Geneva University Hospital
Geneva, Canton of Geneva, 1211, Switzerland
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Jean-Paul Janssens, M.D.
Centre antituberculeux
Study Design
- Study Type
- observational
- Observational Model
- CASE ONLY
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
Study Record Dates
First Submitted
November 13, 2007
First Posted
November 14, 2007
Study Start
October 1, 2004
Study Completion
January 1, 2006
Last Updated
November 14, 2007
Record last verified: 2007-11