CLINICAL_TRIALS ClinicalTrials.gov record update

Prospective Multicenter Study on the Identification of Genetic Abnormalities Predisposing to Vasospasm From a Privileged Model: the Primary Raynaud's Phenomenon

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT02202291
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:37:40.553259+00:00
Published At: 2020-06-24T00:00:00+00:00
Record Updated At: 2020-06-24
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: ["Primary Raynaud\u0027s Phenomenon (PR)", "Genetic Mutations Causing PR", "Study of Patients and Their Relatives (With or Without Primary PR)"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2020-06-24"
protocolSection.identificationModule.nctId: "NCT02202291"
protocolSection.identificationModule.officialTitle: "Prospective Multicenter Study on the Identification of Genetic Abnormalities Predisposing to Vasospasm From a Privileged Model: the Primary Raynaud\u0027s Phenomenon"
protocolSection.statusModule.overallStatus: "COMPLETED"
protocolSection.designModule.phases: ["NA"]
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.

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