Quantiferon for Detection of Latent Tuberculosis in Healthcare Workers (QUANTIPS)
Primary Purpose
Tuberculosis
Status
Completed
Phase
Phase 4
Locations
France
Study Type
Interventional
Intervention
Quantiferon Gold
Sponsored by
About this trial
This is an interventional diagnostic trial for Tuberculosis focused on measuring Occupational Diseases, Tuberculosis, Tuberculin Test, Immunoassay
Eligibility Criteria
INCLUSION CRITERIA:
Group 1:
- Healthcare worker volunteering for the study
- Stable (expected employment in the unit > one year)
- Working in a high-risk units for tuberculosis (at least 5 cases of smear-positive pulmonary tuberculosis per year)
Group 2 :
- Healthcare worker volunteering for the study
- With an unexpected exposure to a patient with contagious tuberculosis (delay in respiratory isolation of a smear-positive patient)
EXCLUSION CRITERIA:
- No informed consent
- Age < 18 years
- Employment in this unit < one year
Sites / Locations
- CHU Bichat Claude Bernard
Arms of the Study
Arm 1
Arm Type
Experimental
Arm Label
Quantiferon Gold
Arm Description
Outcomes
Primary Outcome Measures
Therapeutic impact of tuberculosis screening using QFTG compared to TST. The impact is defined by the decision to treat of not a HCW with latent tuberculosis using QFTG, compared to the decision which would have been based on TST alone
Secondary Outcome Measures
Cost-effectiveness of replacing TST by QFTG
Prevalence and incidence of latent tuberculosis in exposed HCWs (Group 1)
Incidence of latent tuberculosis in HCWs exposed to an index case (Group 2)
Full Information
NCT ID
NCT00797836
First Posted
November 24, 2008
Last Updated
January 9, 2012
Sponsor
Assistance Publique - Hôpitaux de Paris
1. Study Identification
Unique Protocol Identification Number
NCT00797836
Brief Title
Quantiferon for Detection of Latent Tuberculosis in Healthcare Workers
Acronym
QUANTIPS
Official Title
Cost-effectiveness of Quantiferon Gold in VITRO Test of T-lymphocytic Response for Detection of Latent Tuberculosis in At-risk Healthcare Workers
Study Type
Interventional
2. Study Status
Record Verification Date
November 2008
Overall Recruitment Status
Completed
Study Start Date
November 2008 (undefined)
Primary Completion Date
October 2010 (Actual)
Study Completion Date
November 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Assistance Publique - Hôpitaux de Paris
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The accuracy of tuberculin skin test (TST) for detecting latent tuberculosis is limited in countries with a high proportion of population having received vaccination with the BCG. We aim to determine the cost-effectiveness of Quantiferon gold (QTFG), compared to BCG vaccine to detect latent tuberculosis in exposed healthcare workers (HCWs)
Detailed Description
The QUANTIPS study includes two components:
survey of HCWs working in high-risk units (respiratory diseases or infectious diseases with at least 5 case of smear-positive pulmonary tuberculosis par year) from 14 University hospitals in France
Follow-up of HCWs with unexpected exposure to a patient with contagious tuberculosis (delay in respiratory isolation of a smear-positive patient) in 4 University hospitals Main objective: Therapeutic impact of tuberculosis screening using TST compared to QFTG. The impact is defined by the decision to treat of not a HCW with latent tuberculosis using QFTG, compared to the decision which would have been based on TST alone
Secondary objectives:
Cost-effectiveness of replacing TST by QFTG
Prevalence and incidence of latent tuberculosis in exposed HCWs (Part 1)
Incidence of latent tuberculosis in HCWs exposed to an index case (part 2) Inclusion: HCWs who volunteer to participate in units with at least 5 patients with smear-positive tuberculosis each year (Group 1), HCWs exposed to a smear-positive patient non isolated at hospital admission (Group 2) Study population: 2000 (Group 1) and 600 (Group 2) HCWs Study duration: inclusion during 3 months, follow-up of one year (Group 1 ); Inclusion for one year, with a 3-month follow up (Group 2)
Study exams:
Group 1 : TST, QFTG, chest radiography at baseline and after one year
Group 2 : TST, QFTG, chest radiography at baseline (within 3 weeks after exposure) and after 3 months
Endpoints:
therapeutic decision regarding tuberculosis treatment, with a cost-effectiveness analysis (Markov's modelling)
prevalence and incidence of latent tuberculosis
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Tuberculosis
Keywords
Occupational Diseases, Tuberculosis, Tuberculin Test, Immunoassay
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Phase 4
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
1024 (Actual)
8. Arms, Groups, and Interventions
Arm Title
Quantiferon Gold
Arm Type
Experimental
Intervention Type
Procedure
Intervention Name(s)
Quantiferon Gold
Other Intervention Name(s)
Interferon-gama, evaluating tuberculosis-specific T-lymphocytic response
Intervention Description
Interferon-gama release assay evaluating tuberculosis-specific T-lymphocytic response
Health Personnel Hospitals, General Occupational Diseases/*epidemiology/*statistics & numerical data Occupational Exposure/*statistics & numerical data
Tuberculosis/*diagnosis/*epidemiology/prevention & control Immunologic Tests/methods/*standards Disease Transmission, Horizontal/*statistics & numerical data Patient Isolation
Tuberculin Test/standards/*methods Immunoassay/methods/*standards T-Lymphocytes/immunology Interferon Type II/*blood/*analysis
*Reagent Kits, Diagnostic
Mass Screening/*methods Incidence Follow-Up Studies Comparative Study Sensitivity and Specificity Risk Assessment/*methods
Primary Outcome Measure Information:
Title
Therapeutic impact of tuberculosis screening using QFTG compared to TST. The impact is defined by the decision to treat of not a HCW with latent tuberculosis using QFTG, compared to the decision which would have been based on TST alone
Time Frame
18 months
Secondary Outcome Measure Information:
Title
Cost-effectiveness of replacing TST by QFTG
Time Frame
18 months
Title
Prevalence and incidence of latent tuberculosis in exposed HCWs (Group 1)
Time Frame
18 months
Title
Incidence of latent tuberculosis in HCWs exposed to an index case (Group 2)
Time Frame
18 months
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
INCLUSION CRITERIA:
Group 1:
Healthcare worker volunteering for the study
Stable (expected employment in the unit > one year)
Working in a high-risk units for tuberculosis (at least 5 cases of smear-positive pulmonary tuberculosis per year)
Group 2 :
Healthcare worker volunteering for the study
With an unexpected exposure to a patient with contagious tuberculosis (delay in respiratory isolation of a smear-positive patient)
EXCLUSION CRITERIA:
No informed consent
Age < 18 years
Employment in this unit < one year
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Guislaine CARCELAIN, Dr
Organizational Affiliation
Assistance Publique - Hôpitaux de Paris
Official's Role
Study Chair
Facility Information:
Facility Name
CHU Bichat Claude Bernard
City
Paris
State/Province
Ile de France
ZIP/Postal Code
75018
Country
France
12. IPD Sharing Statement
Citations:
PubMed Identifier
25682769
Citation
Lucet JC, Abiteboul D, Estellat C, Roy C, Chollet-Martin S, Tubach F, Carcelain G; QUANTIPS Study Group. Interferon-gamma release assay vs. tuberculin skin test for tuberculosis screening in exposed healthcare workers: a longitudinal multicenter comparative study. Infect Control Hosp Epidemiol. 2015 May;36(5):569-74. doi: 10.1017/ice.2015.19. Epub 2015 Feb 16.
Results Reference
derived
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Quantiferon for Detection of Latent Tuberculosis in Healthcare Workers
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