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Medical and Economical Impact of IGRAs Diagnosis of Latent Tuberculosis in HIV-infected Patients

Medical and Economical Evaluation of New Diagnosis Tests of Mycobacterium Tuberculosis, Specific Immune Responses in HIV-infected Adults

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00805272
Acronym
IGRAVIH
Enrollment
536
Registered
2008-12-09
Start date
2009-02-28
Completion date
2012-02-29
Last updated
2012-03-19

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV, Latent Tuberculosis Infection, Tuberculosis

Keywords

HIV, tuberculosis, IGRA, diagnosis, treatment naive

Brief summary

Tuberculosis is a current infection during HIV infection. After infectious contact, some patients will develop tuberculosis some will only be infected without symptoms, they have Latent Tuberculosis Infection (LTBI) which can reactivate later.In order to prevent this tuberculosis reactivation, LTBI diagnosis screening is preconised in HIV-infected patients. This diagnosis is made till now by the tuberculin skin test (TST) but this test is not specific of TB. New blood tests (QFTB-G and T-SPOT.TB) specific po MTB infection are now sold but have not been evaluated in immunocompromised HIV-infected patients. The primary endpoint of this study is the evaluation of the theoretic therapeutic impact of the use of IGRAS for diagnosis of LTBI in HIV-infected patients

Detailed description

Principal outcome: -Theoretic therapeutic impact evaluation of the use of IGRAS for diagnosis of LTBI in HIV-infected patients . Secondary outcomes: * Medico-economic impact of replacement of TST by IGRAs in LTBI screening in HIV infected patients. * Concordance of IGRAs results with TST * Concordance between IGRAs. * Concordance between IGRAs in accordance to CD4 number(\< 100, 100 à 200, 200 à 300, \> à 300/mm3). * LTBI prevalence in the study group. * Effective consequences of tests results on therapeutic outcome of the patients LTBI criteria and therapeutic recommendations * One or 2 positive IGRAs test: LTBI recommended to be LTBI * 1 negative IGRAs test and one undetermined : no LTBI * 2 undetermined: * No clinical risk and negative TST: no diagnosis, eventually new test at 3 months or after HAART onset. * Clinical risk or TST\> 10mm: LTBI recommended to be treated. Therapeutic outcome evaluation Effective consequences of IGRA's result on patients outcome at 6 months. Analyzed criteria: Therapeutic impact: * Patients percentage with different therapeutic outcome based on usual recommendations * Medico-economic impact * Medico-economic impact of both tests as early and late cost - efficacy * Statistics Primary criteria: * Percentage of patients for whom therapeutic would have been changed by IGRAs results compared to usual diagnosis strategy. Secondary criteria: * Concordance of IGRAs with TST * Concordance between both IGRAs. * Taille: 1000 patients Timing: -inclusions: 2 years

Interventions

OTHERQTF-TB Gold and T-SPOT TB

evaluation of the theoric therapeutic impact of the use of IGRAS for diagnosis of LTBI in HIV-infected patients

Sponsors

Assistance Publique - Hôpitaux de Paris
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

18 yrs old Confirmed HIV infection No HAART Consent signed 6 months follow-up possible

Exclusion criteria

Confirmed TB disease No social right pregnancy

Design outcomes

Primary

MeasureTime frame
To evaluate the theoretical therapeutic impact (in terms of CHIMIOPROPHYLAXIE antituberculous theoretically managed) of the tracking of tuberculosis-latent by QTF-TB Gold IT® or T-SPOT.TB among patients HIV.J0

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 4, 2026