Viewing Study NCT04433520


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Ignite Modification Date: 2025-12-26 @ 3:03 AM
Study NCT ID: NCT04433520
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2025-03-27
First Post: 2020-06-12
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Trevisio Post-Approval Study
Sponsor: Abbott Medical Devices
Organization:

Study Overview

Official Title: Amplatzer™Trevisio™Delivery System Post-Approval Study
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2025-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: TrevisioPAS
Brief 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.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: False
Is a FDA Regulated Device?: True
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: True
Is an FDA AA801 Violation?: