Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
500 participants
OBSERVATIONAL
2005-01-31
2006-09-30
Brief Summary
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Any Adverse Events including, Sever rash, Severe Hepatitis, Lipid abnormalities, Severe Anemia and Other, common AEs will be analysed.
Detailed Description
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Conditions
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Keywords
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Study Design
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DEFINED_POPULATION
OTHER
Interventions
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Highly Active Antiretroviral Treatment (combination of :NRTI, NNRTI,or PI)
Eligibility Criteria
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Inclusion Criteria
* Age \>15 years.
* informed consent
Exclusion Criteria
15 Years
ALL
No
Sponsors
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Rajavithi Biomolecular Research Center
OTHER
Department of Medical Services Ministry of Public Health of Thailand
OTHER_GOV
Principal Investigators
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Subsai Kongsaengdao, M.D.
Role: PRINCIPAL_INVESTIGATOR
Department of Medical Services Ministry of Public Health of Thailand
Locations
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Rajavithi Hospital
Bangkok, , Thailand
Lumpang Hospital
Lumpang, , Thailand
Sappasithiprasong Hospital
Ubonratchathani, , Thailand
Countries
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Other Identifiers
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RVH_CER_003
Identifier Type: -
Identifier Source: org_study_id