Tuberculosis Clinical Trial
— CADOOLOfficial title:
Active Close Contact Investigation of Tuberculosis Through Computer-aided Detection and Stool Xpert MTB/RIF Among People Living in Oromia Region, Ethiopia: a Prospective, Cross-sectional Study (CADOOL Study)
Tuberculosis is the 13th cause of death from all causes, infecting roughly the 25% of the world population, and Ethiopia is listed among the 30 high-burden countries both for TB and for HIV/TB. In recent years, the immediate consequence of the COVID-19 pandemic was a large fall in the number of newly reported TB cases indicators that represent a relevant drawback in the pursue of the 2025 End TB Milestones. For active case investigation of TB close contacts, WHO recently recommended the use of Computer- aided detection (CAD), a technology that can help chest X-ray interpretation in situations of human resources constrains, and it may be cost-effective in low-resource settings. Also, for tuberculosis diagnosis, widely-available GeneXpert on stool samples showed high diagnostic performances in term of both sensitivity and specificity. It is important to assess alternative modalities that could improve diagnosis during TB contact investigation in Ethiopia and the other countries where TB represents a crucial burden.
Status | Not yet recruiting |
Enrollment | 231 |
Est. completion date | December 31, 2024 |
Est. primary completion date | December 31, 2023 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 4 Years and older |
Eligibility | Inclusion Criteria: - All patients diagnosed with pulmonary tuberculosis and at least one sputum sample positive for acid- fast bacilli on sputum smear or M. tuberculosis on sputum Xpert or smear will be eligible for inclusion as index cases. - Index cases will be recruited both among hospitalized patients and patients followed in OPD clinics for completion of TB treatment. - All household contacts of at least 4 years of age will be eligible for inclusion if they lived in the same dwelling as the index patient during the two months prior to the diagnosis of the index patient. - Pregnant women are eligible for the inclusion but, to minimize radiation exposure risk to the fetus, chest X-ray will not be offered. Exclusion Criteria: - Household contacts already receiving treatment for active or latent tuberculosis will be excluded from the study. |
Country | Name | City | State |
---|---|---|---|
Ethiopia | St Luke Hospital | Wolisso, Oromia |
Lead Sponsor | Collaborator |
---|---|
Doctors with Africa - CUAMM | Armauer Hansen Research Institute, Ethiopia, University of Bari |
Ethiopia,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Other | Clinical TB diagnosis rate | The additional positive cases when information from CAD4TB is available to the clinician. | 12 weeks | |
Other | Tuberculosis False positive rate | The false positive cases when information from CAD is available to the clinician | through study completion, an average of 1 year | |
Other | Discordant diagnosis case rate | The number and type of discordant cases in CAD4TB vs. clinician CXR evaluation. | 12 weeks | |
Primary | CAD4TB and Stool GeneXpert Accurancy rate for Diagnosis of TB | The common accuracy metrics (sensitivity, specificity, positive and negative predictive values) when assessing the accuracy of CAD4TB compared to stool Xpert MTB/RIF. | through study completion, an average of 1 year | |
Secondary | Stool GeneXpert and Sputum GeneXpert concordance | The concordance between stool GeneXpert and sputum GeneXpert. | 12 weeks | |
Secondary | Concordance beetwen CAD4TB and Sputum MTB/RIF | The common accuracy metrics (sensitivity, specificity, positive and negative predictive values) when assessing the accuracy of CAD4TB compared to Xpert MTB/RIF | through study completion, an average of 1 year | |
Secondary | TB incidence rate | The incidence of new TB cases among participants during the study period. | through study completion, an average of 1 year |
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