CLINICAL_TRIALS ClinicalTrials.gov record update

Identification of Genes Causing Familial ALS or Increasing Risk for Sporadic ALS and ALS With Frontotemporal Dementia and Understanding Disease Mechanism.

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT00821132
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:38:50.011145+00:00
Published At: 2023-01-26T00:00:00+00:00
Record Updated At: 2023-01-26
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: ["Amyotrophic Lateral Sclerosis (ALS)", "Familial Amyotrophic Lateral Sclerosis", "ALS With Frontotemporal Dementia (ALS/FTD)", "Lou Gehrig\u0027s Disease", "Motor Neuron Disease (MND)", "Primary Lateral Sclerosis (PLS)", "Sporadic ALS (SALS)"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2023-01-26"
protocolSection.identificationModule.nctId: "NCT00821132"
protocolSection.identificationModule.officialTitle: "Identification of Genes Causing Familial ALS or Increasing Risk for Sporadic ALS and ALS With Frontotemporal Dementia and Understanding Disease Mechanism."
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: []
protocolSection.statusModule.resultsFirstPostDateStruct.date: ""

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