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RECRUITINGOBSERVATIONAL

Prevention ICONA Dedicated Ensemble

Implementation of an Italian Cohort of People on HIV-1 Pre-exposure Prophylaxis Within the ICONA Network: PrIDE (Prevention ICONA Dedicated Ensemble)

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

About This Trial

Despite significant advances in HIV treatment, transmission remains a public health concern. In 2022, there were 1.3 million new HIV infections worldwide and 1,888 new diagnoses in Italy, with sexual transmission being the predominant route. Many individuals are still diagnosed late, and a portion of people living with HIV are unaware of their status. Pre-Exposure Prophylaxis (PrEP) has emerged as an effective biomedical strategy to prevent new infections, especially when integrated into comprehensive prevention efforts. Study Objectives The primary objective of this observational study is to establish a large prospective cohort of individuals using PrEP in Italy. The study aims to assess PrEP's effectiveness, tolerability, adherence, and barriers to long-term use in a real-world setting. These data will be instrumental in guiding future strategic interventions to optimize PrEP management and move toward the goal of zero new HIV infections in Italy. Primary Objective * To assess the incidence of new HIV infections among PrEP users in Italy. Secondary Objectives * Incidence of other sexually transmitted infections (STIs); * Tolerability of PrEP; * Psychological and behavioral aspects related to PrEP use; * Adherence and persistence in care; * Use of therapies and prophylaxis for STIs during PrEP use. Study Design and Coordination This is a prospective observational study, promoted by Fondazione ICONA in collaboration with clinical centers and community-based organizations. The coordinating enrolling center is INMI "L. Spallanzani" IRCCS in Rome. Participating Centers: * 49 university and hospital-based centers across Italy; * 4 non-clinical checkpoints offering PrEP screening, prescription, and follow-up. Study Population Adults (≥18 years) who are HIV-negative, sexually active, and considered eligible for PrEP per national or international guidelines, including both new and current PrEP users. Inclusion Criteria * Age ≥18 years; * Negative HIV test at enrollment; * Willingness to initiate or continue PrEP; * Informed consent provided. Exclusion Criteria * HIV infection or strong suspicion of infection; * Contraindications to PrEP medications; Known allergy to PrEP components; Refusal to comply with study procedures.

Who May Be Eligible (Plain English)

Who May Qualify: - Age \>18 years - Negative HIV Ab/Ag test (4th generation or higher) at the enrollment visit - Request and/or willingness to take PrEP, or already on PrEP - Ability to understand the study procedures and to sign willing to sign a consent form Who Should NOT Join This Trial: - Individuals with HIV infection or with strong clinical/epidemiological suspicion of HIV infection - Individuals with contraindications to the use of medications included in the PrEP regimen (as per the product information) - Documented allergy to one or more pharmacological components of the proposed PrEP regimen - Lack of willingness to adhere to the required procedures and follow-up assessments Always talk to your doctor about whether this trial is right for you.

Original Eligibility Criteria

View original clinical language
Inclusion Criteria: * Age \>18 years * Negative HIV Ab/Ag test (4th generation or higher) at the enrollment visit * Request and/or willingness to take PrEP, or already on PrEP * Ability to understand the study procedures and to sign informed consent Exclusion Criteria: * Individuals with HIV infection or with strong clinical/epidemiological suspicion of HIV infection * Individuals with contraindications to the use of medications included in the PrEP regimen (as per the product information) * Documented allergy to one or more pharmacological components of the proposed PrEP regimen * Lack of willingness to adhere to the required procedures and follow-up assessments

Locations (20)

Ospedale Clinicizzato SS. Annunziata - Scuola di Specializzazione di Malattie Infettive
Chieti, Abruzzo, Italy
Ospedale Civile Santo Spirito - U.O. Malattie Infettive
Pescara, Abruzzo, Italy
AOU Consorziale - Policlinico Giovanni XXIII - Struttura Complessa di Malattie Infettive
Bari, Apulia, Italy
A.O.U. Ospedali Riuniti di Foggia - U.O.C. di Malattie Infettive
Foggia, Apulia, Italy
Ospdale San Carlo
Potenza, Basilicate, Italy
Università della Campania Luigi Vanvitelli - Malattie Infettive
Caserta, Campania, Italy
A.O.U. Federico II - U.O.C. di Malattie Infettive
Naples, Campania, Italy
Azienda Ospedaliera dei Colli - Monaldi Cotugno CTO - IV Divisione, U.O.C. di Immunodeficienze e Malattie Infettive di Genere
Naples, Campania, Italy
Presidio Ospedaliero A.O.U. Vanvitelli - U.O. di Malattie Infettive
Naples, Campania, Italy
A.O.U. Policlinico S. Orsola-Malpighi, Università degli Studi di Bologna - U.O. di Malattie Infettive
Bologna, Emilia-Romagna, Italy
BLQ Check Point
Bologna, Emilia-Romagna, Italy
A.O.U. di Ferrara - Arcispedale Sant'Anna - U.S. Gestione Ambulatorio HIV/AIDS U.O. Malattie Infettive
Ferrara, Emilia-Romagna, Italy
Università degli Studi di Modena e Reggio Emilia, Modena - Clinica di Malattie Infettive e Tropicali
Modena, Emilia-Romagna, Italy
Azienda Ospedaliera Arcispedale Santa Maria Nuova - U.O. Malattie Infettive
Reggio Emilia, Emilia-Romagna, Italy
Azienda Ospedaliera Universitaria Friuli Centrale (ASU FC) Santa Maria della Misericordia - Clinica Malattie Infettive
Udine, Friuli Venezia Giulia, Italy
Università Sapienza Polo Pontino - U.O. di Malattie Infettive
Latina, Lazio, Italy
Circolo Mario Mieli
Rome, Lazio, Italy
INMI "L. Spallanzani" IRCCS - U.O.C. Immunodeficienze Virali
Rome, Lazio, Italy
Roma Check Point
Rome, Lazio, Italy
Università Cattolica del Sacro Cuore - Istituto di Clinica delle Malattie Infettive
Rome, Lazio, Italy