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

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Record identity and dates

Source

ClinicalTrials.gov

Source record ID

NCT03613948

Title field or adapter rule

protocolSection.identificationModule.officialTitle

Ingested At

2026-04-28T10:38:26.242618+00:00

Published At

2021-10-25T00:00:00+00:00

Record Updated At

2021-10-25

Timestamp Basis

source retrieval time was not retained by the feed adapter

Date limitation

source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions

["Inherited Retinal Dystrophy Primarily Involving Sensory Retina", "Inherited Retinal Dystrophy Primarily Involving Retinal Pigment Epithelium"]

protocolSection.statusModule.lastUpdatePostDateStruct.date

"2021-10-25"

protocolSection.identificationModule.nctId

"NCT03613948"

protocolSection.identificationModule.officialTitle

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

protocolSection.statusModule.overallStatus

"COMPLETED"

protocolSection.designModule.phases

[]

protocolSection.statusModule.resultsFirstPostDateStruct.date

""

Study condition terms

• Inherited Retinal Dystrophy Primarily Involving Sensory Retina (protocolSection.conditionsModule.conditions)
• Inherited Retinal Dystrophy Primarily Involving Retinal Pigment Epithelium (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

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