Actively Recruiting

Age: 18Years +
All Genders
ID00411983

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

Led by The HIV Netherlands Australia Thailand Research Collaboration · Updated on 2025-03-17

10000

Participants Needed

1

Research Sites

N/A

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are conducting a long-term observational study to understand the outcomes of people living with HIV who have participated in previous HIV-NAT trials. This study aims to provide insights into the long-term safety and durability of different antiretroviral treatments, the effectiveness of HIV viral load and CD4 cell counts in predicting disease progression and mortality, and the impact of adherence to treatment. It also seeks to explore various complications and quality of life over an extended period. The study follows participants who were previously or are currently involved in HIV-NAT trials, collecting and evaluating ongoing clinical outcomes. It assesses long-term consequences related to different antiretroviral drug classes, including risks of metabolic issues like lipodystrophy, resistance patterns, and effects on various body systems such as cardiovascular, renal, and hepatic functions. The study also monitors opportunistic infections or malignancies among co-infected patients and evaluates immune recovery and quality of life. Participants provide written consent and their health is monitored over a period that can extend up to 30 years. The study involves regular evaluations of clinical outcomes, adherence to medication, and quality of life assessments. Researchers analyze data to better understand long-term effects and disease progression in HIV, helping to inform future treatment approaches and patient care strategies.

CONDITIONS

Brief Title

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

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • HIV infected patients (children and adults) who previously participated in HIV-NAT studies
  • HIV infected patients (children and adults) currently participating in HIV-NAT trials
  • Able to provide written consent
Not Eligible

You will not qualify if you...

  • Unable to provide written consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

Long-term Monitoring

Duration - Up to 30 years

Participants who previously participated in HIV-NAT studies are observed over a long period to collect and evaluate clinical outcomes related to HIV infection and treatment effects.

Trial Site Locations

Total: 1 location

1

HIV-NAT, Thai Red Cross AIDS Research Center

Bangkok, Thailand, 10330

Actively Recruiting

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Research Team

A

Anchalee Avihingsanon, MD, PhD

S

Stephen Kerr, PhD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

0

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Published Research Related To This Trial

Impact of viral hepatitis co-infection on response to antiretroviral therapy and HIV disease progression in the HIV-NAT cohort.

W Phillip Law, Chris J Duncombe, Apicha Mahanontharit...

https://pubmed.ncbi.nlm.nih.gov/15166532

Risk of severe hepatotoxicity associated with antiretroviral therapy in the HIV-NAT Cohort, Thailand, 1996-2001.

W Phillip Law, Gregory J Dore, Chris J Duncombe...

https://pubmed.ncbi.nlm.nih.gov/14523276

Short communication: Aging not gender is associated with high atazanavir plasma concentrations in Asian HIV-infected patients.

Anchalee Avihingsanon, Stephen J Kerr, Baralee Punyawudho...

https://pubmed.ncbi.nlm.nih.gov/24088045

Monitoring the toxicity of antiretroviral therapy in resource limited settings: a prospective clinical trial cohort in Thailand.

Reto Nuesch, Preeyaporn Srasuebkul, Jintanat Ananworanich...

https://pubmed.ncbi.nlm.nih.gov/16895939

Factors associated with daily tenofovir exposure in Thai subjects taking combination antiretroviral therapy.

Stephen J Kerr, Baralee Punyawudho, Narukjaporn Thammajaruk...

https://pubmed.ncbi.nlm.nih.gov/25384393

Ergotism in Thailand caused by increased access to antiretroviral drugs: a global warning.

Anchalee Avihingsanon, Reshmie A Ramautarsing, Gompol Suwanpimolkul...

https://pubmed.ncbi.nlm.nih.gov/24531557

Advanced liver fibrosis by transient elastography, fibrosis 4, and alanine aminotransferase/platelet ratio index among Asian hepatitis C with and without human immunodeficiency virus infection: role of vitamin D levels.

Anchalee Avihingsanon, Salyavit Jitmitraparp, Pisit Tangkijvanich...

https://pubmed.ncbi.nlm.nih.gov/24730732