Evaluation of Clinical Progression, Prognostic Factors, and Quality of Life in Patients with Age-related Macular Degeneration.

NCT ID: NCT06899360

Last Updated: 2025-03-27

Basic Information

• Recruitment Status: RECRUITING
• Total Enrollment: 200 participants
• Study Classification: OBSERVATIONAL
• Study Start Date: 2024-10-01
• Study Completion Date: 2029-10-01

Brief Summary

The VERA-AMD study is a prospective, observational study designed to evaluate clinical progression, prognostic factors, and quality of life in patients with age-related macular degeneration (AMD). The study aims to analyze real-world clinical data to identify key predictors of disease progression and functional outcomes, with the goal of optimizing AMD management. The study involves 200 patients aged ≥50 with a confirmed diagnosis of AMD, monitored through routine clinical practice. Primary outcomes include progression rates to advanced AMD and changes in visual acuity, while secondary outcomes focus on retinal morphology and quality of life. Anti-VEGF therapy and AI-based fluid analysis will be integrated to explore their impact on disease progression and patient outcomes.

Detailed Description

The VERA-AMD study is a prospective, non-interventional, observational study investigating the clinical course, prognostic factors, and quality of life in patients with age-related macular degeneration (AMD). AMD is a leading cause of vision loss among the elderly, manifesting as either neovascular ("wet") AMD (nAMD) or geographic atrophy ("dry") AMD (GA-AMD). Despite advances in treatment, there is considerable variability in disease progression and response to therapy. This study aims to fill this gap by analyzing real-world data to identify predictors of disease progression and functional outcomes, ultimately improving clinical management strategies.

Study Objectives

The study's main objectives are to:

Assess the clinical progression of AMD in routine clinical practice. Identify prognostic factors associated with favorable or unfavorable disease outcomes.

Evaluate the impact of AMD on patient quality of life using validated questionnaires.

Methodology

Design: Prospective, non-profit, observational study. Population: 200 patients aged ≥50 years with confirmed AMD in at least one eye. Inclusion Criteria: Confirmed diagnosis of AMD, scheduled follow-up according to clinical practice.

Exclusion Criteria: Significant ocular or systemic diseases affecting visual outcomes.

Outcomes

Primary Outcome: Progression rate to advanced AMD, expressed as cases per 100 patient-years.

Secondary Outcomes: Changes in visual acuity, retinal morphology assessed by optical coherence tomography (OCT), and patient-reported quality of life.

Anti-VEGF Therapy and AI-Based Fluid Analysis

A significant part of the study focuses on the role of anti-VEGF treatment in controlling disease progression, especially in nAMD. Anti-VEGF agents such as aflibercept and ranibizumab are standard treatments for neovascular AMD, aiming to reduce fluid accumulation and neovascularization. The study will explore the relationship between treatment regimens (fixed vs. as-needed dosing) and clinical outcomes, including visual acuity and anatomical changes.

Artificial intelligence (AI)-based analysis of retinal fluid dynamics will be employed using OCT imaging data. Machine learning algorithms will be applied to identify patterns in fluid accumulation and disease progression, improving early detection and personalized treatment approaches.

Data Collection and Statistical Analysis

Data will be collected through regular clinical visits, OCT imaging, and visual acuity testing. Statistical analysis will include repeated measures models to evaluate disease progression and predictors of clinical outcomes. Sample size calculations anticipate a 5.2% annual progression rate in early/intermediate AMD and a 19.7% rate in advanced AMD, with an 80% statistical power at a 0.05 significance level.

Timeline

Interim analysis after 12 months (50 patients with follow-up). Primary analysis after 12 months (all patients). Follow-up analysis at 36 months. Consent and Ethics

Informed consent will be obtained from all participants. Data will be anonymized and handled according to ethical guidelines and institutional review board (IRB) protocols.

Conditions

Age-Related Macular Degeneration

Study Design

• Observational Model Type: COHORT
• Study Time Perspective: OTHER

Study Groups

Observational cohort of patients with age-related macular degeneration

Observational cohort of patients with age-related macular degeneration eventually receiving anti-VEGF agents as per clinical practice.

No interventions assigned to this group

Eligibility Criteria

Inclusion Criteria

• age ≥ 50 years.
• confirmed diagnosis of AMD in at least one eye.
• follow-up scheduled according to standard clinical practice.

Exclusion Criteria

• presence of other significant ocular conditions that could affect visual acuity.
• systemic conditions that make the patient unsuitable for long-term follow-up.

• Minimum Eligible Age: 50 Years
• Maximum Eligible Age: 120 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

University of Udine

OTHER

Sponsor Role: lead

Responsible Party

Daniele Veritti

Prof.

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Daniele Veritti

Role: PRINCIPAL_INVESTIGATOR

Department of Ophthalmology, University of Udine

Locations

Department of Ophthalmology

Udine, UD, Italy

Site Status: RECRUITING

Countries

Italy

Central Contacts

Daniele Veritti

Role: CONTACT

daniele.veritti@uniud.it

+390432559907

Facility Contacts

Daniele Veritti

Role: primary

daniele.veritti@uniud.it

+390432559907

Other Identifiers

OCU_DMED_2025_1

Identifier Type: -

Identifier Source: org_study_id