Status:
COMPLETED
Left Atrial Appendage Ligation Using the Atriclip Device
Lead Sponsor:
St. Helena Hospital Coon Joint Replacement Institute
Collaborating Sponsors:
AtriCure, Inc.
Adventist Heart and Vascular Institute
Conditions:
Left Atrial Appendage Ligation
Eligibility:
All Genders
21+ years
Brief Summary
The purpose of the study is to collect data regarding ligation of the left atrial appendage at least 12 months after surgery for patients that had exclusion of the left atrial appendage as a primary m...
Detailed Description
The purpose of this study is to collect data regarding ligation of the left atrial appendage at least 12 months after surgery for patients that had exclusion of the left atrial appendage as a primary ...
Eligibility Criteria
Inclusion
- All adult patient who had a heart procedure where an Atriclip device was deployed as the primary or secondary procedure between 3/2013-12/20/2016
- Patient is willing to undergo a trans esophageal echocardiogram, or if unable a CT angiogram
- If female, must be of non-childbearing potential or have a negative pregnancy test within 7 days prior to the procedure
- Patient is willing to sign an IRB approved Informed Consent
Exclusion
- Patient did not have an Atriclip device as part of the surgical procedure between 3/2013 and 12/2016.
- Patient is unwilling or unable to undergo trans esophageal echocardiogram with general anesthesia or a CT angiogram
Key Trial Info
Start Date :
April 1 2016
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
April 1 2018
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT03759418
Start Date
April 1 2016
End Date
April 1 2018
Last Update
November 30 2018
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