Clinical Trials Directory

Trials / Recruiting

RecruitingNCT00411983

A Long-term Follow-up of the HIV-NAT Cohort

A Long-term Follow-up Study for HIV-infected Individuals Who Have Participated in HIV-NAT Study Protocols

Status
Recruiting
Phase
Study type
Observational
Enrollment
10,000 (estimated)
Sponsor
The HIV Netherlands Australia Thailand Research Collaboration · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

With HIV/AIDS increasingly considered a chronic disease, 24-, or 48-week data from antiretroviral studies are no longer sufficient. Only with long-term follow-up and outcome data will shed some much-needed light on the answers of questions that have stumped us for several years. Data from a large observational cohort of patients treated with combination antiretroviral therapy will provide further insights into the long-term safety and durability of various antiretroviral therapeutic approached, the efficacy of HIV viral load and CD4 cell counts as predictors of disease progression and mortality, and the importance of adherence.

Detailed description

Primary Objective: To collect and evaluate long-term clinical outcomes of HIV infected participants previously enrolled in HIV-NAT trials. Secondary Objective: To Assess: 1. Long-term consequences of initiation of antiretroviral as predicted by baseline CD4 cell count and/or baseline plasma HIV RNA level 2. Incidence of lipodystrophy and other metabolic complications in three different groups of patients initially treated with NRTI-based regimens, NNRTI-based regimens, or PI-based regimens 3. Class-specific incidence of lipodystrophy and metabolic complications such as d4T versus AZT, nevirapine versus efavirenz and individual PIs (IDV, SQV, Kaletra, and atazanavir) 4. Resistance profiles in patients on different antiretroviral regimens 5. Long-term consequences of antiretroviral agents on cardiovascular, renal, hepatic, and endocrine function, skin, gastrointestinal system and urogentital tract 6. Incidence of opportunistic infections or malignancy including hepatocarcinoma in patients with HIV/HCV or HIV/HBV co-infection 7. Immune recovery syndrome 8. Adherence to different antiretroviral regimens 9. Quality of life

Conditions

Timeline

Start date
2002-11-01
Primary completion
2030-12-01
Completion
2030-12-01
First posted
2006-12-15
Last updated
2025-03-17

Locations

1 site across 1 country: Thailand

Source: ClinicalTrials.gov record NCT00411983. Inclusion in this directory is not an endorsement.