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NCT04745624: VASCADE

Real World Use and Outcomes of VASCADE Closure Device Versus Manual Compression in Patients With CFA Disease

Completed Last updated 3 February 2022
What this trial tests

trial in Common Femoral Artery Stenosis in 200 participants. Completed in 1 December 2021.

Timeline
20 August 2020
Primary endpoint
1 December 2021
1 December 2021

Quick facts

Lead sponsorYale University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment200
Start date20 August 2020
Primary completion1 December 2021
Estimated completion1 December 2021
Sites1 location across United States

Conditions studied

Sponsor

Yale University

Who can join

Adults 18 to 100, any sex, with Common Femoral Artery Stenosis. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

To study the patient characteristics and outcomes associated with the real-world use of manual compression vs. vascular closure devices (VCDs) after common femoral artery (CFA) percutaneous access for coronary and endovascular interventions. An institutional procedural database, based on electronic medical record information will be abstracted to collect this information.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other recruiting trials for Common Femoral Artery Stenosis

Currently open trials in the same condition.

Other Yale University trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04745624.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing