Viewing Study NCT01240902


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Study NCT ID: NCT01240902
Status: COMPLETED
Last Update Posted: 2022-10-25
First Post: 2010-11-10
Is NOT Gene Therapy: False
Has Adverse Events: True

Brief Title: Safety and Efficacy Study of the Medtronic CoreValveĀ® System in the Treatment of Symptomatic Severe Aortic Stenosis in High Risk and Very High Risk Subjects Who Need Aortic Valve Replacement
Sponsor: Medtronic Cardiovascular
Organization:

Study Overview

Official Title: Medtronic CoreValveĀ® U.S. Pivotal Trial
Status: COMPLETED
Status Verified Date: 2022-10
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: None
Brief Summary: The purpose of the study is to evaluate the safety and efficacy of the Medtronic CoreValveĀ® System in the treatment of symptomatic severe aortic stenosis in subjects who have a predicted high risk for aortic valve surgery and/or very high risk for aortic valve surgery.
Detailed Description: None

Study Oversight

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