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Clinical Trials in Italy / NCT06747754
Starting soon Observational

HIV Database (DBHIV)-Establishment of a Database of HIV Patients

NCT06747754 · tracked via the Priya Life Science Italy tracker
Phase
Observational
Started
2025-01-01
Last updated
2024-12-24

Condition(s) studied

HIV Infections

Investigational drug(s) / intervention(s)

Establishment of a Database of HIV Patients

Establishment of a Database of HIV Patients: Establishment of a database that allows for systematic and continuous collection of data relating to clinical, laboratory and treatment characteristics of patients with HIV-1 for research purposes.

Study summary

In Italy, there are over 90,000 patients with HIV-1 infection on antiretroviral therapy (ART). The availability of different classes of antiretroviral drugs (nucleoside and non-nucleoside reverse transcriptase inhibitors (NRTIs, NNRTIs), protease inhibitors (PIs), integrase inhibitors (INSTIs) and viral entry inhibitors (IEs) that act in different phases of the HIV life cycle, together with careful patient management, has allowed us to obtain long-lasting therapeutic efficacy in the vast majority of Italian patients, making this infection a chronic disease.The introduction of combination antiretroviral therapy (cART) has completely revolutionized the management of HIV-positive patients, drastically reducing HIV-associated mortality and morbidity. In fact, the course of HIV infection has transformed into a chronic disease, and the number of HIV-infected patients over 50 years of age has increased significantly and the number of elderly subjects is progressively increasing. Furthermore, HIV infection seems to accelerate the aging process, causing immune system dysfunction, excess oxidative stress and increased inflammatory processes (inflammaging).

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * Age \>18 years * Patients with chronic HIV infection (certified by a positive test for the detection of anti-HIV antibodies) * Ability to sign the informed consent or signature of the declaration in lieu of consent in the case of deceased patients Exclusion Criteria: * lack of willingness to provide free and informed consent.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Fondazione Policlinico Universitario A. Gemelli IRCCS, UOC Malattie Infettive Rome Lazio

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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 NCT06747754 on ClinicalTrials.gov ↗ ← All trials in Italy