Status:
COMPLETED
Specificity Trial of the Recombinant Tuberculosis Allergen in BCG Vaccinated Healthy Volunteers
Lead Sponsor:
National Medical Research Center of Phthisiopulmonology and Infectious Diseases
Conditions:
Tuberculosis
Eligibility:
All Genders
18-30 years
Phase:
NA
Brief Summary
The aim of this study is to test the recombinant tuberculosis skin test in the previously BCG vaccinated healthy adults with low risk of TB development, to determine the test specificity.
Detailed Description
Recombinant tuberculosis allergen (RTA) is a recombinant fusion protein CFP10-ESAT6 produced by the prokaryotic cell line. The test is widely used in Russian Federation and CIS countries for the laten...
Eligibility Criteria
Inclusion
- Signed informed consent for the participation in the study.
- Age 18 to 30 years
- A history of BCG vaccination (confirmed by medical documentation and/or the presence of BCG scar)
- Healthy individual according to physical examination and medical records at screening.
- Willingness to cooperate and follow the recommendations of the Investigator in accordance with the Protocol.
Exclusion
- A history of tuberculosis or close contact with a patient with active tuberculosis for 5 years prior to the enrollment in the study.
- Positive T-SPOT.TB test at the enrollment in the study
- Treatment with drugs affecting immune system within 3 months prior to the enrollment in the study
- Vaccination against any infections \<1.5 months prior to the enrollment in the study
- Vaccination with BCG \<6 months prior to the enrollment in the study.
- The Mantoux test with 2 TU and/or the test with the recombinant tuberculosis allergen was performed less than 6 months prior to the enrollment in the study.
- Congenital or acquired immunodeficiency.
- Active disease of the immune system
- HIV infection.
- The current condition of the skin interferes with the conduct and reading of skin tests (trauma, skin diseases).
- A disease in which blood sampling poses a risk to the volunteer (hemophilia, other bleeding disorders) or obstructed venous access.
- The volunteer currently participates in another clinical study or has participated in another clinical study within 3 months prior to the enrollment in the study.
- Previous participation in clinical studies of ESAT-6 and/or CFP-10 antigens.
- Pregnancy, lactation, pregnancy planning.
- The reluctance of a female person to use effective barrier (including spermicidal gel), hormonal or intrauterine contraceptives during the study.
- History of alcohol, drug, benzodiazepine, or other substance abuse within the 12 months prior to the enrollment in the study.
- Use of alcoholic beverages within 24 hours prior to the visit.
- A condition or disease that, in the opinion of the Investigator, is inappropriate for participation in the study.
Key Trial Info
Start Date :
November 24 2021
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
January 26 2022
Estimated Enrollment :
150 Patients enrolled
Trial Details
Trial ID
NCT05203068
Start Date
November 24 2021
End Date
January 26 2022
Last Update
August 25 2023
Active Locations (1)
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1
National Medical Research Center of Phthisiopulmonology and Infectious Diseases
Moscow, Russia