NCT Number: NCT00367731
NOW Thai HAART Study
After Initiation of HAART in peoples who living with HIV/AIDS in Thailand by the year 2000, rapidly expanded HAART access of national project has been promoted in 2004. Free ARVs (For CD4<200cell/cu.mm. or in symptomatic HIV with CD4<250 cell/cu.mm. )and CD4 monitoring has been available. The first-line regimen is d4T+3TC+NVP in mainly the first time (Naive) patients. CD4 response ), rate of opportunistic infection, and neurological outcomes were measured. Rate of ARV change, adverse events,treatment failure, TB co-infection rate, percent changing to EFV-based regimen or PI-based regimen were recorded.
Any Adverse Events including, Sever rash, Severe Hepatitis, Lipid abnormalities, Severe Anemia and Other, common AEs will be analysed.
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Notify MeKey information
Conditions
Age range
15 year and older
Sex eligibility
All sexes
Study type
Observational
Primary location
Rajavithi Hospital, Bangkok, Thailand
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
- HIV/AIDS patients.
- Age >15 years.
- informed consent
Exclusion criteria
- Not informed consent
Treatment and study plan
Sponsors and collaborators
Lead sponsor
Department of Medical Services Ministry of Public Health of Thailand
Other Gov
Collaborators
- Rajavithi Biomolecular Research Center
Registry information
Official study title
Neurological Outcomes With in THAI National HAART Program.
Important dates
- Study start
- 2005
- Study completion
- 2006
- First posted
- Aug 23, 2006
- Registry last updated
- Aug 23, 2006
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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