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Left Atrial Appendage Ligation Using the Atriclip Device

NCT03759418 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 100

Last updated 2018-11-30

No results posted yet for this study

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 minimally invasive procedure or in conjunction with other open cardiac or minimally invasive cardiac procedures.

Conditions

  • Left Atrial Appendage Ligation

Interventions

DEVICE

exclusion of the left atrial appendage

A trans esophageal echocardiogram will be performed to assess the Atriclip device in the closure of the left atrial appendage in patients that had surgery at least 12 months ago.

Sponsors & Collaborators

  • AtriCure, Inc.

    collaborator INDUSTRY

  • Adventist Heart and Vascular Institute

    collaborator UNKNOWN

  • St. Helena Hospital Coon Joint Replacement Institute

    lead OTHER

Principal Investigators

  • Gansevoort Dunnington, MD · St. Helena Hospital Adventist Heart Institute

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-04-30
Primary Completion
2018-04-30
Completion
2018-04-30

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03759418 on ClinicalTrials.gov