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

NCT03613948 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 280

Last updated 2021-10-25

No results posted yet for this study

Summary

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."

Conditions

  • Inherited Retinal Dystrophy Primarily Involving Sensory Retina
  • Inherited Retinal Dystrophy Primarily Involving Retinal Pigment Epithelium

Sponsors & Collaborators

  • Gangnam Severance Hospital

    lead OTHER

Principal Investigators

  • Jinu Han · Gangnam Severance Hospital

Eligibility

Min Age
4 Months
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2018-04-10
Primary Completion
2021-01-20
Completion
2021-01-20

Countries

  • South Korea

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 NCT03613948 on ClinicalTrials.gov