HIV Clinical Trial
This study aims to estimate the prevalence of bridging liver fibrosis and cirrhosis (METAVIR score ≥ F2) according to METAVIR score in HIV infected patients not chronically infected by viral hepatitis but exhibiting a metabolic syndrome according to the IDF definition (International Diabetes Foundation).
HIV-associated morbidity and mortality has been considerably modified ever since the
availability of potent antiretroviral treatment in 1996. Recent studies have shown the
impact of treatment, with the decreased frequency of AIDS-related diseases coinciding with
the preponderance of non-AIDS related pathologies.
Consequently, diseases of hepatic origin have become a key problem in the therapeutic course
of HIV-infected patients, representing a major source of significant morbidity and
mortality. Liver-related diseases comprise of various etiologies, including co-infection
with chronic viral hepatitis and excessive alcohol consumption. When excluding these
particular diseases, fibrotic patients exhibit an elevated prevalence of metabolic syndrome,
regardless of lipodystrophy. Directly linked to metabolic syndrome, non-alcoholic hepatic
steatosis has the capacity to induce necro-inflammatory lesions with an increased risk of
evolving into cirrhosis and its complications thereto (i.e. hepatocellular carcinoma, liver
decompensation, and end-stage liver disease). In the context of HIV, very little data is
available concerning the link between metabolic syndrome and hepatic fibrosis, despite the
increasing risk of developing such disease during extended life-span, the long-term
disruption of glycolipid metabolism induced by antiretroviral treatment, and the presence of
various social risk-factors (i.e. increasing trends in weight gain and decreased physical
activity).
The principal objective of the present study is to then characterize the prevalence and
determinants associated with hepatic fibrosis among HIV-infected patients, without
co-infection with other hepatitis viruses, and who present symptoms of metabolic syndrome
according to the AHA 2009 definition. In order to more appropriately answer this research
question, we will conduct a nested, matched case-control study including 300 HIV-infected
patients per group. We will also aim to identify risk-factors of liver fibrosis other than
metabolic syndrome, to study agreement in 4 non-invasive scores of liver fibrosis and 3
non-invasive score of steatosis, and to evaluate the performance of the Controlled
Attenuation Parameter (CAP) method for use in diagnosing hepatic steatosis.
All patients in this study will be recruited in a clinical center situated in the infectious
disease unit at Saint-Antoine Hospital, where 3400 HIV-infected patients have regular
consultations. Patients will be identified from an in-house informatics platform, serving as
a surveillance tool for metabolic syndrome, among other diseases, with the intention of
increasing better-adapted clinical and therapeutic care. Each patient presenting with
metabolic syndrome will be matched with a control patient on the following characteristics:
age (±5 years), duration of HIV-infection (±2 years), HIV-RNA viral load (in categories of
<50-500, 501-1000, or >1000 copies/mL), and gender. Patients with abnormal transaminases
will be excluded from this study.
This study will bring about a clearer understanding of the frequency and importance of liver
fibrosis risk in patients with metabolic syndrome, which will allow us to determine the more
important elements of surveillance necessary in the prevention and development of hepatic
lesions. Accordingly, this study will add more pertinent information regarding treatment
guidelines specific to this patient population.
;
Observational Model: Case Control, Time Perspective: Cross-Sectional
Status | Clinical Trial | Phase | |
---|---|---|---|
Recruiting |
NCT06162897 -
Case Management Dyad
|
N/A | |
Completed |
NCT03999411 -
Smartphone Intervention for Smoking Cessation and Improving Adherence to Treatment Among HIV Patients
|
Phase 4 | |
Completed |
NCT02528773 -
Efficacy of ART to Interrupt HIV Transmission Networks
|
||
Active, not recruiting |
NCT05454839 -
Preferences for Services in a Patient's First Six Months on Antiretroviral Therapy for HIV in South Africa
|
||
Recruiting |
NCT05322629 -
Stepped Care to Optimize PrEP Effectiveness in Pregnant and Postpartum Women
|
N/A | |
Completed |
NCT02579135 -
Reducing HIV Risk Among Adolescents: Evaluating Project HEART
|
N/A | |
Active, not recruiting |
NCT01790373 -
Evaluating a Youth-Focused Economic Empowerment Approach to HIV Treatment Adherence
|
N/A | |
Not yet recruiting |
NCT06044792 -
The Influence of Primary HIV-1 Drug Resistance Mutations on Immune Reconstruction in PLWH
|
||
Completed |
NCT04039217 -
Antiretroviral Therapy (ART) Persistence in Different Body Compartments in HIV Negative MSM
|
Phase 4 | |
Active, not recruiting |
NCT04519970 -
Clinical Opportunities and Management to Exploit Biktarvy as Asynchronous Connection Key (COMEBACK)
|
N/A | |
Completed |
NCT04124536 -
Combination Partner HIV Testing Strategies for HIV-positive and HIV-negative Pregnant Women
|
N/A | |
Recruiting |
NCT05599581 -
Tu'Washindi RCT: Adolescent Girls in Kenya Taking Control of Their Health
|
N/A | |
Active, not recruiting |
NCT04588883 -
Strengthening Families Living With HIV in Kenya
|
N/A | |
Completed |
NCT02758093 -
Speed of Processing Training in Adults With HIV
|
N/A | |
Completed |
NCT02500446 -
Dolutegravir Impact on Residual Replication
|
Phase 4 | |
Completed |
NCT03805451 -
Life Steps for PrEP for Youth
|
N/A | |
Active, not recruiting |
NCT03902431 -
Translating the ABCS Into HIV Care
|
N/A | |
Completed |
NCT00729391 -
Women-Focused HIV Prevention in the Western Cape
|
Phase 2/Phase 3 | |
Recruiting |
NCT05736588 -
Elimisha HPV (Human Papillomavirus)
|
N/A | |
Recruiting |
NCT03589040 -
Darunavir and Rilpivirine Interactions With Etonogestrel Contraceptive Implant
|
Phase 2 |