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Same-Day Antiretroviral Therapy Initiation

The Thai Red Cross AIDS Research Centre

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT04032028
Enrollment
2500
Registered
2019-07-25
Start date
2018-04-01
Completion date
2025-12-01
Last updated
2024-11-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

HIV Infections

Brief summary

Data from a total of 2,500 walk-in or referred individuals who have been confirmed (diagnosed) HIV positive and accessing care and treatment services at the hospitals targeted by this study will be examined. The starting period for this project is estimated to be the last quarter (Q4) of fiscal year 2018.

Detailed description

This 24-month observation study will be conducted in 13 hospitals of 5 provinces in Thailand: Chiang Rai, Chiang Mai, Ubon Ratchathani, Chonburi, and Songkhla. The research team of TRCARC will collect and analyze secondary and de-identified data from the hospitals' databases. In each site, clients who agree to receive Same-Day ART service will go through standard of care procedures at each hospital, which include: post-test counseling and psychosocial support, baseline lab test, clinical screening, and physical examination. The drug regimen prescribed for clients will mirror the first line ART regimen in Thailand's national guideline, which is tenofovir (TDF), emtricitabine (FTC), and efavirenz (EFV). Retention of the clients will reflect that of the hospital's protocol, and CD4 and viral load will be tested according to the national guideline.

Interventions

None listed

Sponsors

Thai Red Cross AIDS Research Centre
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL

Inclusion criteria

1. Thai nationals 2. HIV-positive status 3. Acceptance of Same-Day ART

Exclusion criteria

1\. not Acceptance of Same-Day ART

Design outcomes

Primary

MeasureTime frameDescription
Acceptance5 yearsAcceptance of Same-Day ART
Type of Clients5 yearsType of Clients (newly diagnosed or re-engaged)
Number of clients categorized by demographic characteristics5 yearsDemographic Characteristics: age (years), gender (sex at birth and gender identity), risk behavior(s), and reason(s) for HIV testing
Number of clients with each clinical characteristic5 yearsClinical Characteristics based on Thailand's national guidelines (anti-HIV, creatinine, alanine transaminase, syphilis serology, hepatitis B antigen, hepatitis C antibodies, urinalysis, chest X-ray, CD4 count, CDC stage, comorbidity)
Number of clients with each ART drug regimen differ from first line ART regimen5 yearsDrug regimen, if different from first line drug (TDF, FTC, EFV)
Duration between date of HIV diagnosis and date of ART initiation5 yearsDuration between date of HIV diagnosis and date of ART initiation
Number of clients with each clinical exclusion criteria5 yearsClinical exclusion criterias : suspected TB, suspected cryptococcal meningitis, suspected serious OIs
Duration between date of ART initiation to date of being successfully transferred and date of ART continuation5 yearsDuration of linkage to care, if applicable (date of being successfully transferred and date of ART continuation)
Retention5 yearsRetention (retention in care, discontinued ART, loss to follow-up, death) at month 1, month 3, month 6, and month 12 after ART initiation
Viral load count5 yearsViral load count (VL tested, percentage of VL suppressed, and dates of VL suppressed)

Countries

Thailand

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 13, 2026