CLINICAL_TRIALS ClinicalTrials.gov record update

Early Feasibility Study of the Vivasure PerQseal®+ (PerQseal® Plus) Vascular Closure Device When Used to Achieve Hemostasis of Common Femoral Arteriotomies Created by 14 to 22 F Sheaths in Patients Undergoing Percutaneous Transcatheter Procedures

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Record identity and dates

Source: ClinicalTrials.gov
Source record ID: NCT05163548
Title field or adapter rule: protocolSection.identificationModule.officialTitle
Ingested At: 2026-04-28T10:39:12.239121+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

protocolSection.conditionsModule.conditions: ["Percutaneous Large Hole Vascular Closure"]
protocolSection.statusModule.lastUpdatePostDateStruct.date: "2023-04-26"
protocolSection.identificationModule.nctId: "NCT05163548"
protocolSection.identificationModule.officialTitle: "Early Feasibility Study of the Vivasure PerQseal\u00ae+ (PerQseal\u00ae Plus) Vascular Closure Device When Used to Achieve Hemostasis of Common Femoral Arteriotomies Created by 14 to 22 F Sheaths in Patients Undergoing Percutaneous Transcatheter Procedures"
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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