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Cohort study of AIDS among drug-users in Guangxi

A cohort study on selective effect of opioids on first-line drugs resistance evolution of HIV-1

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR1800017416
Enrollment
Unknown
Registered
2018-07-29
Start date
2014-06-01
Completion date
Unknown
Last updated
2018-08-20

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

Conditions

Drug-resistance of HIV

Interventions

Opioid HIV+ group:none
Non-Opioid HIV+ group:none

Sponsors

Guangxi Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
19 Years to 87 Years

Inclusion criteria

Inclusion criteria: 1. Opioid HIV+ group (1) Aged 18 years or older male and female; (2) Han / Zhuang people; (3) History of drug abuse / methadone use; (4) AIDS status: HIV+; (5) Viral load: > 1000cp/ml; (6) Status of hiv treatment: no / has been treated with HAART. 2. Non-Opioid HIV+ group (1) Aged 18 years or older male and female; (2) Han / Zhuang people; (3) No history of drug abuse / methadone use; (4) AIDS status: HIV+; (5) Viral load: > 1000cp/ml; (6) Status of hiv treatment: no / has been treated with HAART.

Exclusion criteria

Exclusion criteria: 1. Opioid HIV+ group (1) Risk factor:They discontinued methadone for more than 15 consecutive days or breaks for more than 30 days in the past 6 months; (2) Health status: major chronic diseases (heart, kidney, lung, endocrine, metabolic or autoimmune diseases and tuberculosis). 2. Non-Opioid HIV+ group (1) Risk factor:Addicted to any kind of drug; (2) Health status: major chronic diseases (heart, kidney, lung, endocrine, metabolic or autoimmune diseases and tuberculosis).

Design outcomes

Primary

MeasureTime frame
HIV-1 drug resistance mutation;

Countries

China

Contacts

Public ContactHuang Jiegang

Guangxi Medical University

jieganghuang@gxmu.edu.cn+86 13878833650

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026