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NCT05258032: RADIS

Structural and Functional Characterization of Rare Ocular Diseases

Status unknown Last updated 15 March 2022
What this trial tests

trial in Retinitis Pigmentosa in 50 participants. Status unknown.

Timeline
24 November 2021
Primary endpoint
24 November 2024
24 November 2025

Quick facts

Lead sponsorBarcelona Macula Foundation
StatusStatus unknown
Study typeOBSERVATIONAL
Enrollment50
Start date24 November 2021
Primary completion24 November 2024
Estimated completion24 November 2025
Sites1 location across Spain

Conditions studied

Sponsor

Barcelona Macula Foundation

Who can join

18 and older, any sex, with Retinitis Pigmentosa or Stargardt Disease 1. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Rare ocular diseases (ROD) are a heterogeneous group of ocular diseases that affect very few people and, generally, for which no tretament is available. An important subgroup of these diseases are inherited retinal degenerations. In this study we focus on understanding the natural history of different ROD that affect the posterior segment.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Retinitis Pigmentosa

Currently open trials in the same condition.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT05258032.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing