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The Thai Red Cross AIDS Research Centre
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.
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.
Age
All ages
Sex
ALL
Healthy Volunteers
No
Thai Red Cross AIDS Research Centre
Pathum Wan, Bangkok, Thailand
Wat Yannasangwararam Hospital
Bang Lamung, Changwat Chon Buri, Thailand
Queen Savang Vadhana Memorial Hospital
Chon Buri, Changwat Chon Buri, Thailand
Sunpasitthiprasong Hospital
Udon Thani, Changwat Ubon Ratchathani, Thailand
Hangdon Hospital
Hang Dong, Chiang Mai, Thailand
Nakornping Hospital
Mae Rim, Chiang Mai, Thailand
Sarapee Hospital
Saraphi, Chiang Mai, Thailand
Hat Yai Hospital
Hat Yai, Song Khla, Thailand
Sanpatong Hospital
Chiang Mai, Thailand
Chiang Mai Hospital
Chiang Mai, Thailand
Start Date
April 1, 2018
Primary Completion Date
July 1, 2022
Completion Date
December 1, 2025
Last Updated
November 25, 2024
2,500
ESTIMATED participants
Lead Sponsor
Thai Red Cross AIDS Research Centre
NCT06694805
NCT04142047
Data Source & Attribution
This clinical trial information is sourced from ClinicalTrials.gov, a service of the U.S. National Institutes of Health.
Modifications: This data has been reformatted for display purposes. Eligibility criteria have been parsed into inclusion/exclusion sections. Location data has been geocoded to enable distance-based search. For the authoritative and most current information, please visit ClinicalTrials.gov.
Neither the United States Government nor Clareo Health make any warranties regarding the data. Check ClinicalTrials.gov frequently for updates.
View ClinicalTrials.gov Terms and ConditionsNCT07428330