Trials / Completed
CompletedNCT02059707
LARIAT RS: An Observational Study of the Performance and Safety of the LARIAT RS
LARIAT RS: An Observational Study of the Performance and Safety of the LARIAT RS Suture Delivery Device
- Status
- Completed
- Phase
- N/A
- Study type
- Interventional
- Enrollment
- 58 (actual)
- Sponsor
- AtriCure, Inc. · Industry
- Sex
- All
- Age
- 21 Years
- Healthy volunteers
- Not accepted
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.
Detailed description
Prospective, observational, single-center, non-randomized study of a stand-alone procedure for the exclusion of the LAA with the LARIAT RS in patients with atrial fibrillation. Completed LAA exclusion will be assessed by TEE.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | LARIAT RS Suture Delivery Device | LARIAT RS Suture Delivery Device |
Timeline
- Start date
- 2014-01-01
- Primary completion
- 2014-12-01
- Completion
- 2015-05-01
- First posted
- 2014-02-11
- Last updated
- 2020-01-09
Locations
1 site across 1 country: Poland
Source: ClinicalTrials.gov record NCT02059707. Inclusion in this directory is not an endorsement.