RecruitingNCT03603977

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

A Simplified Therapy Regimen Study of Lopinavir and Ritonavir Combined With Lamivudine for HIV-1 Infected Patients in the Real World of China


Sponsor

Guangzhou 8th People's Hospital

Enrollment

600 participants

Start Date

Nov 1, 2017

Study Type

OBSERVATIONAL

Conditions

Summary

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


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This observational study is collecting data on people living with HIV in China who have chosen to use a simplified antiretroviral treatment regimen, to better understand how well these simpler treatment approaches work in real-world settings. **You may be eligible if...** - You have been confirmed to have HIV-1 infection - You agree to use a simplified treatment regimen - You agree to have your CD4 count (immune cells) checked at least every six months **You may NOT be eligible if...** - You have participated in an HIV vaccine trial or another drug trial in the past 3 months - You are unlikely to complete all scheduled follow-up visits (due to poor compliance or serious illness) - You have a history of resistance or allergic reaction to the medications used (lopinavir/ritonavir or lamivudine) Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

Interested in this trial?

Get notified about updates and connect with the research team.

Interventions

DRUGLpv/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.


Locations(1)

Guangzhou 8th People's Hospital

Guangzhou, Guangdong, China

View Full Details on ClinicalTrials.gov

For the most up-to-date information, visit the official listing.

Visit

NCT03603977


Related Trials