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NCT03613948

Study on the Effects of Mutations Under Inherited Retinal Disease in Korean

Completed Last updated 25 October 2021
What this trial tests

trial in Inherited Retinal Dystrophy Primarily Involving Sensory Retina in 280 participants. Completed in 20 January 2021.

Timeline
10 April 2018
Primary endpoint
20 January 2021
20 January 2021

Quick facts

Lead sponsorGangnam Severance Hospital
StatusCompleted
Study typeOBSERVATIONAL
Enrollment280
Start date10 April 2018
Primary completion20 January 2021
Estimated completion20 January 2021
Sites1 location across South Korea

Conditions studied

Sponsor

Gangnam Severance Hospital

Who can join

Adults 4 Months to 75, any sex, with Inherited Retinal Dystrophy Primarily Involving Sensory Retina or Inherited Retinal Dystrophy Primarily Involving Retinal Pigment Epithelium. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To develop comprehensive genetic maps of inherited retinal diseases in Korean * Establishment of comprehensive genetic database in Koreans with inherited retinal diseases including frequently mutated genes, genotype-phenotype correlations, and visual prognosis."

Publications & conference data

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

  1. In Silico identification of a common mobile element insertion in exon 4 of RP1.
    Won D, Hwang JY, Shim Y, Byeon SH, et al · · 2021 · cited 10× · PMID 34183725 · DOI 10.1038/s41598-021-92834-4

Verify or expand the search:

Other recruiting trials for Inherited Retinal Dystrophy Primarily Involving Sensory Retina

Currently open trials in the same condition.

Other Gangnam Severance Hospital 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/NCT03613948.

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