Trials / Completed
CompletedNCT01997905
Stroke Feasibility Study
Feasibility Clinical Investigation of a Minimally Invasive Surgically Deployed AtriCure AtriClip Left Atrial Appendage Exclusion System for Stroke Prophylaxis in Patients With Non-Valvular Atrial Fibrillation and in Whom Long Term Oral Anticoagulation Therapy is Medically Contraindicated
- Status
- Completed
- Phase
- Phase 1 / Phase 2
- Study type
- Interventional
- Enrollment
- 13 (actual)
- Sponsor
- AtriCure, Inc. · Industry
- Sex
- All
- Age
- 18 Years – 80 Years
- Healthy volunteers
- Not accepted
Summary
This is a feasibility study to assess the safety and efficacy of the AtriCure AtriClip when placed via Minimally Invasive Surgical Deployment to the Left Atrial Appendage. The purpose is for evaluation of Stroke Prevention in Patients with Non-Valvular Atrial Fibrillation who are unable to take Oral Anticoagulants.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DEVICE | AtriClip LAA Exclusion Device |
Timeline
- Start date
- 2014-01-01
- Primary completion
- 2015-07-01
- Completion
- 2015-08-01
- First posted
- 2013-11-28
- Last updated
- 2016-12-14
- Results posted
- 2016-10-21
Locations
7 sites across 1 country: United States
Source: ClinicalTrials.gov record NCT01997905. Inclusion in this directory is not an endorsement.