Skip to main content
TTrialFinder
TrialFinder is for informational purposes only and does not provide medical advice. Always talk to your doctor.
RECRUITINGOBSERVATIONAL

Screening and Follow-up in Patients With HIV Infection Combined With Metabolic Associated Fatty Liver Disease

Important: This information is not medical advice. Talk to your doctor about whether a clinical trial is right for you.

About This Trial

Identifying patients at risk of NAFLD(Nonalcoholic fatty liver disease), especially severe disease with NASH(nonalcoholic steatohepatitis) and fibrosis, is critical. Prevalence of NAFLD in PLWH(People Living With HIV) evaluated by different imaging techniques including US (ultrasonography), elastography, CT(computed tomography ), and magnetic resonance varies from 13% to 58.6% in all published studies. In previous studies, the effect of ART(Anti-Retroviral Therapy) on NAFLD was limited. A cross-sectional analysis found that INSTI(Integrase strand transfer inhibitor) was associated with a higher prevalence of steatosis in AIDS (acquired immunodeficiency syndrome) patients. However, it is not clear whether there is a difference in the degree of nonalcoholic steatosis between AIDS patients receiving NNRTI(non-nucleoside reverse transcriptase inhibitors). Therefore, the investigators plan to conduct a prospective study to assess whether there is any difference in the degree of nonalcoholic steatosis and fibrosis between Chinese HIV(human immunodeficiency virus)/AIDS patients after initial treatment with NNRTI or INSTI, or switching from NNRTI to INSTI.

Who May Be Eligible (Plain English)

Who May Qualify: - Newly treated or treated AIDS patients; - Regular follow-up visits to the hospital, medication compliance is good; - Patients or their family members were willing to participate in the study by understanding the study plan and providing written willing to sign a consent form. Who Should NOT Join This Trial: - Unable to complete the position requirements of ultrasonic examination (lying flat) due to mobility difficulties; - Patients have poor compliance and cannot follow up regularly or take medicine on time; - Patients or family members cannot understand the conditions and objectives of the study; - Other conditions considered unsuitable for inclusion by the investigator. Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Newly treated or treated AIDS patients; * Regular follow-up visits to the hospital, medication compliance is good; * Patients or their family members were willing to participate in the study by understanding the study plan and providing written informed consent. Exclusion Criteria: * Unable to complete the position requirements of ultrasonic examination (lying flat) due to mobility difficulties; * Patients have poor compliance and cannot follow up regularly or take medicine on time; * Patients or family members cannot understand the conditions and objectives of the study; * Other conditions considered unsuitable for inclusion by the investigator.

Locations (1)

Chinese Academy of Medical Sciences Peking Union Medical College Hospital
Beijing, Beijing Municipality, China