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NCT04195711

Comparative Validation of "Blinq" and "2WIN" Vision Screeners

Completed Last updated 19 October 2020
What this trial tests

trial testing objective pediatric vision screen, "blinq," in Strabismic Amblyopia in 100 participants. Completed in 26 November 2019.

Timeline
18 November 2019
Primary endpoint
26 November 2019
26 November 2019

Quick facts

Lead sponsorAlaska Blind Child Discovery
StatusCompleted
Study typeOBSERVATIONAL
Enrollment100
Start date18 November 2019
Primary completion26 November 2019
Estimated completion26 November 2019
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Alaska Blind Child Discovery

Who can join

Adults 1 to 65, any sex, with Strabismic Amblyopia or Refractive Amblyopia. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

After 28 years of development, the binocular birefringence screener ("blinq," "Rebion") was commercially released. It need to be validated with AAPOS (American Association for Pediatric Ophthalmology and Strabismus) criteria in part because the next Uniform Standards document is pending. Adult and children pediatric and strabismus patients were screened with blinq and "2WIN" photoscreener with "CR" corneal reflex alignment test and then compared to confirmatory exam with age-appropriate determination of binocular status.

Publications & conference data

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

  1. Comparative AAPOS Validation of the Birefringent Amblyopia Screener with Isolated Small-Angle Strabismus.
    Arnold RW. · · 2020 · cited 13× · PMID 32099317 · DOI 10.2147/opth.s242335

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Other Alaska Blind Child Discovery trials

Trials by the same sponsor.

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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/NCT04195711.

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