CLINICAL_TRIALS ClinicalTrials.gov record update

Frequency, Clinical Phenotype and Genetic Analysis of Heritable Kidney Cancer Syndromes

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT05534854
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:39:36.749745+00:00
Published At: 2023-08-31T00:00:00+00:00
Record Updated At: 2023-08-31
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: ["Renal Tumor Histology", "Kidney Cancer", "Renal Cell Carcinoma", "Familial Renal Cancer", "HLRCC", "VHL Syndrome", "BAP1 Tumor Predisposition Syndrome", "FLCN Gene Mutation", "ALK Gene Mutation", "FH Gene Mutation", "Birt-Hogg-Dube Syndrome", "MET Gene Mutation", "Cutaneous Leiomyoma", "Cutaneous Leiomyomata With Uterine Leiomyomata"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2023-08-31"
protocolSection.identificationModule.nctId: "NCT05534854"
protocolSection.identificationModule.officialTitle: "Frequency, Clinical Phenotype and Genetic Analysis of Heritable Kidney Cancer Syndromes"
protocolSection.statusModule.overallStatus: "UNKNOWN"
protocolSection.designModule.phases: []
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

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