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Prospective Analysis of "Genotype-phenotype" Correlations Observed in a Large Cohort of Patients With Hereditary Retinal Dystrophies - GEPHIRD

NCT03662386 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 103

Last updated 2025-12-10

No results posted yet for this study

Summary

This study will carry out a detailed descriptive analysis of a large population of patients with hereditary retinal dystrophies (HRD): clinical, paraclinical and genetic data.

The information drawn from these analyzes will provide a better understanding of the pathophysiology of these rare diseases and this may ultimately impact the medical management of patients (targeted therapy).

Conditions

  • Hereditary Retinal Dystrophies

Interventions

PROCEDURE

OCT-A

Optical coherence tomography angiography (OCT-A)

PROCEDURE

Visual acuity (ETDRS)

Visual acuity tested with ETDRS score (Early Treatment Diabetic Retinopathy Study)

Sponsors & Collaborators

  • Fondation Ophtalmologique Adolphe de Rothschild

    lead NETWORK

Principal Investigators

  • Elise BOULANGER SCEMAMA · Fondation Ophtalmologique A. de Rothschild

Eligibility

Min Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-09-14
Primary Completion
2025-03-14
Completion
2025-03-14

Countries

  • France

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03662386 on ClinicalTrials.gov