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LARIAT RS: An Observational Study of the Performance and Safety of the LARIAT RS

NCT02059707 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 58

Last updated 2020-01-09

No results posted yet for this study

Summary

The objective is to assess the effectiveness of permanent exclusion of the LAA with the LARIAT RS Suture Delivery Device and accessories in AF patients.

Conditions

  • Atrial Appendage

Interventions

DEVICE

LARIAT RS Suture Delivery Device

LARIAT RS Suture Delivery Device

Sponsors & Collaborators

  • AtriCure, Inc.

    lead INDUSTRY

Study Design

Allocation
NA
Purpose
BASIC_SCIENCE
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
21 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2014-01-31
Primary Completion
2014-12-31
Completion
2015-05-31

Countries

  • Poland

Study Locations

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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 NCT02059707 on ClinicalTrials.gov