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Recruiting Observational

Simplified Treatment of Anti-retrovirus in China (C-STAR)

NCT03603977 · tracked via the Priya Life Science China tracker
Phase
Observational
Started
2017-11-01
Last updated
2022-09-14

Condition(s) studied

HIV/AIDS

Investigational drug(s) / intervention(s)

Lpv/r+3TCAll LPV/r trials (3) →All Gammora trials (5) →

Lpv/r+3TC: It is a simplified therapy regimen study of lopinavir and ritonavir combined with lamivudine for HIV-1 infected patients in the real world of China.

Study summary

To observe the efficacy and safety of simplified therapy regimen for treating with HIV-1 infected patients in Chinese real word.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: 1. HIV-1 infection confirmed 2. Agree to use simplified therapy regimen. 3. Agree to detect CD4 count at least once per half a year Exclusion Criteria: 1. Have participated in HIV vaccine clinical trial or other drug trials in the past three months. 2. Patients who could not complete the scheduled follow-up (such as weakness and poor compliance). 3. Patients who have the history of resistance or allergy to LPV/r or 3TC.

Primary outcome measure(s)

  • The rate of virus inhibition — 36 Months
    the ratio of HIV RNA\< 50 copies/mL at 12, 24 or 36 months after treatment.

Trial sites (1)

FacilityCityRegionStatus
Guangzhou 8th People's Hospital Guangzhou Guangdong Recruiting
Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT03603977 on ClinicalTrials.gov ↗ ← All trials in China