CLINICAL_TRIALS ClinicalTrials.gov record update

SNP-based Microdeletion and Aneuploidy RegisTry

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: NCT02381457
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:37:50.964959+00:00
Published At: 2021-01-29T00:00:00+00:00
Record Updated At: 2021-01-29
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: ["22q11 Deletion Syndrome", "DiGeorge Syndrome", "Trisomy 21", "Trisomy 18", "Trisomy 13", "Monosomy X", "Sex Chromosome Abnormalities", "Cri-du-Chat Syndrome", "Angelman Syndrome", "Prader-Willi Syndrome", "1p36 Deletion Syndrome"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2021-01-29"
protocolSection.identificationModule.nctId: "NCT02381457"
protocolSection.identificationModule.officialTitle: "SNP-based Microdeletion and Aneuploidy RegisTry"
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.

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