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NCT05190146Completed

Epidemiologic Study to Assess the IGRA Positivity in Populations With a High TB Burden

A Multi-country, Epidemiologic Study to Assess the Interferon Gamma Release Assay (IGRA) Positivity, and to Build Capacity to Conduct a Tuberculosis (TB) Vaccine Efficacy Study, in Populations With a High TB Disease Burden

Source: ClinicalTrials.gov · Last updated 13 Dec 2024

Brief summary (registry, in English)

The purpose of this study is to conduct a multi-country, multi-site, epidemiologic study designed to assess the proportion of interferon gamma release assay (IGRA) positivity, at site level, and to build capacity to conduct a future TB vaccine efficacy study.

Status (registry)
Completed
Study type
Observational
Enrollment
7203 (actual)
First submitted
29 Nov 2021
Start date
20 Dec 2021
Primary completion date
11 Sept 2023
Lead sponsor
Gates Medical Research Institute
Diseases
Tuberculosis
NCT number
NCT05190146

What you commit to

  • Study type: Observational
  • Participants enrolled: 7203
  • From 20 Dec 2021 to the primary completion date, 11 Sept 2023
  • 36 sites in 14 countries
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • History of previous administration of an experimental Mtb vaccine

Other illness

  • History of active TB within the last 24 months (i.e., 24 months from end of treatment to day of screening, based on history \[no documentation required\])
  • Unstable / uncontrolled chronic condition according to the judgment of the investigator

Other

  • \-

Who the study is looking for

  • Between 15 and 34 years of age (inclusive)
  • Participants who agree to stay in contact with the study site for the duration of the study, provide updated contact information as necessary, and have no current plans to relocate from the study area for the duration of the study.

Age in the registry: 15 years to 34 years · Sex: All · Accepts healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (36)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Investigational Site
Coordinator of this site? Confirm its status
DhakaBangladeshUnknown status
Investigational Site
Coordinator of this site? Confirm its status
Porto AlegreBrazilUnknown status
Investigational Site
Coordinator of this site? Confirm its status
Rio de JaneiroBrazilUnknown status
Investigational Site
Coordinator of this site? Confirm its status
BaktiIndonesiaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
BandungIndonesiaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
PersabahanIndonesiaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
PuneIndiaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
KisumuKenyaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
MombasaKenyaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
NairobiKenyaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
ManicaMozambiqueUnknown status
Investigational Site
Coordinator of this site? Confirm its status
MaputoMozambiqueUnknown status
Investigational Site
Coordinator of this site? Confirm its status
ComasPeruUnknown status
Investigational Site
Coordinator of this site? Confirm its status
LimaPeruUnknown status
Investigational Site
Coordinator of this site? Confirm its status
DasmariñasPhilippinesUnknown status
Investigational Site
Coordinator of this site? Confirm its status
Iloilo CityPhilippinesUnknown status
Investigational Site
Coordinator of this site? Confirm its status
Makati CityPhilippinesUnknown status
Investigational Site
Coordinator of this site? Confirm its status
MandaluyongPhilippinesUnknown status
Investigational Site
Coordinator of this site? Confirm its status
Quezon CityPhilippinesUnknown status
Investigational Site
Coordinator of this site? Confirm its status
EntebbeUgandaUnknown status
Investigational Site
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MulagoUgandaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
Hà NộiVietnamUnknown status
Investigational Site
Coordinator of this site? Confirm its status
Ho Chi Minh CityVietnamUnknown status
Investigational Site
Coordinator of this site? Confirm its status
BloemfonteinSouth AfricaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
DurbanSouth AfricaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
GermistonSouth AfricaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
KimberleySouth AfricaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
MtubatubaSouth AfricaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
SoshanguveSouth AfricaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
SowetoSouth AfricaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
Three RiversSouth AfricaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
EmmasdaleZambiaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
LusakaZambiaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
NdolaZambiaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
BanjulThe GambiaUnknown status
Investigational Site
Coordinator of this site? Confirm its status
KinshasaDemocratic Republic of the CongoUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.