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NOW Thai HAART Study

R

Rajavithi Hospital

Status

Completed

Conditions

AIDS
Neurological Complications
HIV

Treatments

Drug: Highly Active Antiretroviral Treatment (combination of :NRTI, NNRTI,or PI)

Study type

Observational

Funder types

Other

Identifiers

NCT00367731
RVH_CER_003

Details and patient eligibility

About

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.

Sex

All

Ages

15+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • HIV/AIDS patients.
  • Age >15 years.
  • informed consent

Exclusion criteria

  • Not informed consent

Trial contacts and locations

3

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Data sourced from clinicaltrials.gov

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