RecruitingNCT07737340

Metabolic Liver Disease in Newly Diagnosed People Living With HIV (MASHIV-TR)

Metabolic Liver Disease in Newly Diagnosed People Living With HIV: MASHIV-TR Cohort (MASHIV-TR)


Sponsor

Yaşar Bayındır, MD

Enrollment

411 participants

Start Date

Jun 1, 2024

Study Type

OBSERVATIONAL

Conditions

Summary

This study aims to identify the risk factors that lead to the development of metabolic liver disease in people who have been newly diagnosed with HIV. The research will take place across 9 centers in Türkiye and plans to include 250 newly diagnosed individuals with HIV, alongside 161 healthy individuals without HIV as a control group. Participants will have their liver health checked when they first join the study (baseline) and then once a year for up to 5 years (at 12, 24, 36, 48, and 60 months). The main goal of these visits is to monitor their metabolic health and understand who is at risk of developing a fatty liver condition known as MASLD (Metabolic dysfunction-Associated Steatotic Liver Disease). During each visit, the research team will collect information about the participants' general health, including their height, weight, medical and family history, lifestyle habits, and sleep patterns. They will also record any medications being taken, including HIV treatments. To thoroughly check liver health, researchers will use routine blood tests (measuring things like cholesterol, blood sugar, and kidney function) and painless, non-invasive imaging tests, such as ultrasounds and FibroScans, to measure liver fat and stiffness.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying Clinical and Laboratory Monitoring, FibroScan (Transient Elastography), and others for people with fatty liver, hiv infections, and other related conditions. The study is currently recruiting participants at 11 locations.

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.

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Interventions

DIAGNOSTIC_TESTFibroScan (Transient Elastography)

Non-invasive measurement of liver stiffness (LSM) and controlled attenuation parameter (CAP) to evaluate liver fibrosis and steatosis. Measurements are taken at baseline and annually up to 60 months.

DIAGNOSTIC_TESTHepatobiliary Ultrasonography (USG)

Routine ultrasound imaging of the liver and biliary tract to evaluate signs of metabolic liver disease and fatty liver. Assessed at baseline and annually up to 60 months.

OTHERClinical and Laboratory Monitoring

Annual monitoring including anthropometric measurements (BMI), lipid profile, fasting glucose, HOMA-IR score, renal and liver function tests, and calculation of the FIB-4 index. For the patient group, details of the initiated Antiretroviral Therapy (ART) will also be recorded.


Locations(11)

Guven Hospital

Ankara, Ankara, Turkey (Türkiye)

Adana Acıbadem Hospital

Adana, Turkey (Türkiye)

Cukurova University, Faculty of Medicine

Adana, Turkey (Türkiye)

Hacettepe University, Faculty of Medicine

Ankara, Turkey (Türkiye)

Akdeniz University, Faculty of Medicine

Antalya, Turkey (Türkiye)

Dicle University, Faculty of Medicine

Diyarbakır, Turkey (Türkiye)

Gaziantep University, Faculty of Medicine

Gaziantep, Turkey (Türkiye)

Health Sciences University Hamidiye Faculty of Medicine

Istanbul, Turkey (Türkiye)

Ege University, Faculty of Medicine

Izmir, Turkey (Türkiye)

Kocaeli University, Faculty of Medicine

Kocaeli, Turkey (Türkiye)

Harran University, Faculty of Medicine

Sanliurfa, Turkey (Türkiye)

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NCT07737340


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