CLINICAL_TRIALS ClinicalTrials.gov record update

Natural History and Genetic Studies of Usher Syndrome

This page presents selected fields from the linked source record. It does not add a medical interpretation.

Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT00106743
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:37:28.904628+00:00
Published At: 2019-12-12T00:00:00+00:00
Record Updated At: 2019-12-12
Timestamp Basis: source retrieval time was not retained by the feed adapter
Date limitation: source retrieval time was not retained by the feed adapter

protocolSection.conditionsModule.conditions: ["Retinitis Pigmentosa Syndromic", "Congenital Deafness", "Usher Syndrome", "Retinitis Pigmentosa and Deafness", "Retinitis Pigmentosa"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2019-12-12"
protocolSection.identificationModule.nctId: "NCT00106743"
protocolSection.identificationModule.officialTitle: "Natural History and Genetic Studies of Usher Syndrome"
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: []
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

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

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.