Tuberculosis, Pulmonary Clinical Trial
Official title:
Primary Prophylaxis for Prevention of TB in Prison's Populations
Verified date | October 2019 |
Source | Federal University of Mato Grosso do Sul |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Interventional |
The purpose of this study is to determine if the isoniazid is effective in the prevention of tuberculosis in a prison population, exposed to the high endemicity of the disease.
Status | Terminated |
Enrollment | 467 |
Est. completion date | August 10, 2019 |
Est. primary completion date | August 10, 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | Male |
Age group | 18 Years to 45 Years |
Eligibility |
Inclusion criteria: - Age above 18 and under 45 at the time of inclusion; - Sign the informed consent form. Exclusion criteria: - Be indigenous; - Active TB or previous use of isoniazid; - Score Alcohol Use Disorders Identification Test =15. - Reactive serology for HIV, hepatitis B and C; - Reactive result for quantiferon, considering as positive the result of Tube 1 and / or Tube22 above 0.2 IU / mL; - Liver enzymes (Aspartate aminotransferase and Alanate aminotransferase) three times the upper limit; - History or treatment for epilepsy; |
Country | Name | City | State |
---|---|---|---|
Brazil | Roberto Oliveira | Dourados | Mato Grosso Do Sul |
Lead Sponsor | Collaborator |
---|---|
Federal University of Mato Grosso do Sul | Oswaldo Cruz Foundation |
Brazil,
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* Note: There are 43 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Quantiferon TB Gold Plus (QIAGEN®) Conversion at the Premature Exclusion Visit. | Number of participants who had a Quantiferon TB Gold Plus (QIAGEN®) score greater than or equal to 0.35 international units per milliliter, at the time of the premature exclusion visit, on all participants in the group. | up to 6 months |
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