Early Feasibility Study of the Vivasure PerQseal® Closure Device System After Use of the Impella Device for Cardiogenic Shock or Protected Percutaneous Coronary Intervention

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Record identity and dates

Source

ClinicalTrials.gov

Source record ID

NCT04818541

Title field or adapter rule

protocolSection.identificationModule.officialTitle

Ingested At

2026-04-28T10:39:12.236759+00:00

Published At

2023-04-26T00:00:00+00:00

Record Updated At

2023-04-26

Timestamp Basis

source retrieval time was not retained by the feed adapter

Date limitation

source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions

["Percutaneous Large Hole Vascular Closure"]

protocolSection.statusModule.lastUpdatePostDateStruct.date

"2023-04-26"

protocolSection.identificationModule.nctId

"NCT04818541"

protocolSection.identificationModule.officialTitle

"Early Feasibility Study of the Vivasure PerQseal\u00ae Closure Device System After Use of the Impella Device for Cardiogenic Shock or Protected Percutaneous Coronary Intervention"

protocolSection.statusModule.overallStatus

"COMPLETED"

protocolSection.designModule.phases

["NA"]

protocolSection.statusModule.resultsFirstPostDateStruct.date

""

Study condition terms

• Percutaneous Large Hole Vascular Closure (protocolSection.conditionsModule.conditions)

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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