CLINICAL_TRIALS ClinicalTrials.gov record update

Genes Causing Congenital Ebstein's Anomaly

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: NCT00497705
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:36:30.732891+00:00
Published At: 2017-07-02T00:00:00+00:00
Record Updated At: 2017-07-02
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: ["Heart Septal Defects, Ventricle", "Heart Defects, Congenital", "Double Outlet Right Ventricle", "Truncus Arteriosus, Persistent"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2017-07-02"
protocolSection.identificationModule.nctId: "NCT00497705"
protocolSection.identificationModule.officialTitle: "Genes Causing Congenital Ebstein\u0027s Anomaly"
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.