Last reviewed · How we verify

NCT04725760

Evaluation of the Efficacy of the BrainPort Vision Pro on the Performance of Daily Activities in the Profoundly Blind French Population

Status unknown NA Last updated 10 November 2021
What this trial tests

NA trial testing BrainPort Vision Pro in Blindness in 125 participants. Status unknown.

Timeline
1 October 2020
Primary endpoint
30 September 2022
30 September 2022

Quick facts

Lead sponsorWicab
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposesupportive care
Enrollment125
Start date1 October 2020
Primary completion30 September 2022
Estimated completion30 September 2022
Sites7 locations across France

Drugs / interventions tested

Conditions studied

Sponsor

Wicab

Who can join

8 and older, any sex, with Blindness. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of the study is to evaluate the effectiveness and safety of the BrainPort® Vision Pro, an electronic oral assistive device, in the performance of daily tasks by French persons who have residual vision limited to light perception or less in both eyes.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Gene-agnostic approaches to treating inherited retinal degenerations.
    Chew LA, Iannaccone A. · · 2023 · cited 14× · PMID 37123404 · DOI 10.3389/fcell.2023.1177838

Verify or expand the search:

Other recruiting trials for Blindness

Currently open trials in the same condition.

Verify against primary sources

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/NCT04725760.

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