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Clinical Trial Summary

A single-arm, non-randomized, multi-center clinical study of the Amplatzer™ Trevisio™ Intravascular Delivery System for facilitating percutaneous, transcatheter implantation of the Amplatzer™ Occluder Devices. NOTE: The enrollment for the VSD cohort is still recruiting (3 subjects at this moment); therefore, the overall status of the study is Recruiting.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT04433520
Study type Observational
Source Abbott Medical Devices
Contact Laetitia Beullens
Phone +32 277 46 937
Email laetitia.beullens@abbott.com
Status Recruiting
Phase
Start date September 14, 2020
Completion date October 15, 2025

See also
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Active, not recruiting NCT04029233 - The PROOF Trial - Prospective, Open-label, Multicenter, Non-randomized Investigation on Percutaneous Patent Foramen Ovale (PFO) Closure Using the Occlutech PFO Occluder to Prevent Recurrence of Stroke in Patients With Cryptogenic Stroke and High Risk PFO
Active, not recruiting NCT04349995 - Amplatzer PFO Occluder Post-marketing Surveillance Study
Recruiting NCT06046508 - Migraine With Aura and Patent Foramen Ovale: Identification of Biomarkers to Select Patients In Whom Intervention Would Be Beneficial (MANET)
Recruiting NCT03821129 - GORE® CARDIOFORM Septal Occluder and Antiplatelet Medical Management for Reduction of Recurrent Stroke in Patients With Patent Foramen Ovale (PFO): the REDUCE Post Approval Study N/A
Not yet recruiting NCT06203873 - A Comparison of Biodegradable and Metal Occluders in Patients With PFO and Migraine N/A
Recruiting NCT06033937 - COMPETE Cohort Study
Active, not recruiting NCT04100135 - GORE® CARDIOFORM Septal Occluder Migraine Clinical Study N/A
Recruiting NCT04946734 - Effectivity and Safety of PFO Closure vs Medicine in Alleviating Migraine Phase 3