Status:
UNKNOWN
Diagnosis and Treatment of Co-infection With Human Immunodeficiency Virus /Latent Tuberculosis Infection (HIV/TBL)
Lead Sponsor:
Instituto Nacional de Salud Publica, Mexico
Collaborating Sponsors:
Instituto Nacional de Enfermedades Respiratorias
Instituto Nacional de Ciencias Medicas y Nutricion Salvador Zubiran
Conditions:
Human Immunodeficiency Virus (HIV)
Tuberculosis (TB)
Eligibility:
All Genders
18-60 years
Phase:
PHASE4
Brief Summary
The purpose of this study is to determine of once identified to the subjects infected with human immunodeficiency virus (positive VIH), to diagnose latent Tuberculosis, and to treat her with isoniazid...
Detailed Description
A descriptive analysis of the data will be made. Means and standard deviations for continuous data frequencies for categorical data will be performed. Wilcoxon test Mann-Whitney U test Chi square will...
Eligibility Criteria
Inclusion
- Accept to participate. Informed consent.
- Human Immunodeficiency Virus positive test, documented by Western Blot
- Have not received treatment for latent tuberculosis
- Have not been diagnosed pulmonary tuberculosis (Tbp)
- Normal two chest X-rays, Postern-anterior and left lateral.
Exclusion
- Active tuberculosis
- Previous diagnosis of tuberculosis
- Antecedent of treatment for active o latent tuberculosis
- Contact with TB patient harboring Multidrug resistance or isoniazid resistant isolates of Mycobacterium tuberculosis.
- Abnormal liver enzyme levels
- Hemoglobin below 8 gr/dl
- Allergy or intolerance to isoniazid
- Peripheral neuropathy
- Ingestion of drugs interacting with isoniazid
Key Trial Info
Start Date :
May 1 2010
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
June 1 2013
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT01875952
Start Date
May 1 2010
End Date
June 1 2013
Last Update
June 12 2013
Active Locations (2)
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1
Instituto Nacional de Salud Publica
México, Cuernavaca Morelos, Mexico, 62100
2
Clínica Especializada CONDESA
Mexico City, D.F, Mexico, 06140