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Predicting Disease Progression in Atrial Fibrillation: A Multiparametric Approach for Prognostic Marker Identification and Personalized Patient Management

Predicting Disease Progression in Atrial Fibrillation: A Multiparametric Approach for Prognostic Marker Identification and Personalized Patient Management

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06647914
Acronym
PAMP FA
Enrollment
322
Registered
2024-10-18
Start date
2025-09-03
Completion date
2026-08-31
Last updated
2024-10-18

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Atrial Fibrillation (AF)

Brief summary

This project leverages artificial intelligence (AI) to decipher Atrial Fibrillation (AF) progression and optimize treatment strategies. By recruiting a diverse cohort of 322 AF patients, we will gather a robust multiparametric dataset including clinical, genetic, electrocardiographic, and echocardiographic data. Harnessing AI, we will extract and correlate hidden components within ECG-obtained P-wave data and echocardiographic studies with atrial fibrosis, culminating in an atrial fibrosis score (AFS). The AFS will non-invasively predict fibrosis extent and AF clinical progression, including metrics like rehospitalization, cardiac morbidity, and mortality. Ultimately, this endeavor aims to improve AF patient management, significantly reducing healthcare costs, and enhancing patient quality of life.

Interventions

None listed

Sponsors

Federico II University
CollaboratorOTHER
Irccs Sdn
CollaboratorOTHER
Marche Polytechnic university, Ancona, Italy
CollaboratorUNKNOWN
IRCCS Policlinico S. Donato
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* History of paroxysmal or persistent atrial fibrillation * Clinical indication for Atrial Fibrosis (AF) ablation according to the 2020 ESC Guidelines

Exclusion criteria

* Age below 18 years old * Refusal to sign consent * Noncompliance with the study protocol

Design outcomes

Primary

MeasureTime frameDescription
A composite clinical point used to evaluate the Atrial Fibrosis Score prognostic capabilityPartecipants will be assessed at the baseline and at 6 months and 12 months time points. The AFS Prediction Model Testing will start at 9 months after the beginning of the patients enrollment.The clinical endpoint will be composed by rehospitalization, cardiac morbidity and total mortality data

Contacts

Primary ContactCarlo Pappone, MD, PHD, FACC
carlo.pappone@af-ablation.org+39-0252774260

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026