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AtriCure

AtriCure logo
🇺🇸United States
Ownership
Public
Established
2000-11-01
Employees
1.2K
Market Cap
-
Website
http://www.atricure.com
Introduction

AtriCure, Inc. engages in the development, manufacture, and sale of surgical ablation of cardiac tissue, and systems for the exclusion of the left atrial appendage. Its products include radio frequency (RF) ablation pacing and sensing, cryo, left atrial appendage management, soft tissue dissection, estech surgical instrumentation, and cart configuration. It operates through the following geographical segments: United States, Europe, Asia, and Other International. The company was founded in 1994 and is headquartered in Mason, OH.

Clinical Trials

35

Active:2
Completed:19

Trial Phases

5 Phases

Phase 1:1
Phase 2:5
Phase 3:4
+2 more phases

Drug Approvals

0

Drug Approvals

No drug approvals found

This company may not have drug approvals in our database

Clinical Trials

Distribution across different clinical trial phases (29 trials with phase data)• Click on a phase to view related trials

Not Applicable
18 (62.1%)
Phase 2
5 (17.2%)
Phase 3
4 (13.8%)
Phase 1
1 (3.4%)
Phase 4
1 (3.4%)

BoxX-NoAF Clinical Trial

Not Applicable
Not yet recruiting
Conditions
Post Operative Atrial Fibrillation
Atrial Fibrillation, Postoperative
First Posted Date
2025-05-25
Last Posted Date
2025-05-25
Lead Sponsor
AtriCure, Inc.
Target Recruit Count
960
Registration Number
NCT06989775
Locations
🇨🇦

Hamilton General Hospital, Hamilton, Ontario, Canada

Cryo NerVe Block Extremity AmputatioN RegIStry for Post Operative and pHantom Limb Pain

Recruiting
Conditions
Amputation
Amputation of Lower Limb
Amputation of Upper Limb
Amputation, Limb Loss
Amputation, Traumatic/Surgery
Cryo Analgesia
First Posted Date
2025-04-03
Last Posted Date
2025-08-12
Lead Sponsor
AtriCure, Inc.
Target Recruit Count
2000
Registration Number
NCT06908538
Locations
🇺🇸

Elliot Hospital, Manchester, New Hampshire, United States

Left Atrial Appendage Exclusion for Prophylactic Stroke Reduction Trial

Not Applicable
Active, not recruiting
Conditions
Ischemic Stroke
Systemic Embolism
First Posted Date
2022-07-28
Last Posted Date
2025-08-12
Lead Sponsor
AtriCure, Inc.
Target Recruit Count
6573
Registration Number
NCT05478304
Locations
🇺🇸

Heart Center Research / Huntsville Hospital, Huntsville, Alabama, United States

🇺🇸

HonorHealth Shea Scottsdale Healthcare, Scottsdale, Arizona, United States

🇺🇸

St. Bernard's Heart & Vascular, Jonesboro, Arkansas, United States

and more 139 locations

CONVERGE Post-Approval Study (PAS)

Not Applicable
Recruiting
Conditions
Chronic Atrial Fibrillation
First Posted Date
2022-05-26
Last Posted Date
2025-06-04
Lead Sponsor
AtriCure, Inc.
Target Recruit Count
325
Registration Number
NCT05393180
Locations
🇺🇸

Eisenhower Medical Center, Rancho Mirage, California, United States

🇺🇸

Bridgeport Hospital System, Bridgeport, Connecticut, United States

🇺🇸

Orlando Health, Orlando, Florida, United States

and more 22 locations

HEAL-IST IDE Trial

Not Applicable
Recruiting
Conditions
Inappropriate Sinus Tachycardia
First Posted Date
2022-03-15
Last Posted Date
2025-05-06
Lead Sponsor
AtriCure, Inc.
Target Recruit Count
142
Registration Number
NCT05280093
Locations
🇺🇸

Loma Linda University Health, Loma Linda, California, United States

🇺🇸

Sequoia Hospital, Redwood City, California, United States

🇺🇸

Stanford University, Redwood City, California, United States

and more 23 locations
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News

AtriCure's EPi-Sense System Receives FDA Approval for Long-Standing Persistent Afib Treatment

• AtriCure's EPi-Sense system has gained FDA approval for treating long-standing persistent atrial fibrillation (Afib), offering a new option for a challenging patient population. • The Converge clinical trial demonstrated the superiority of Hybrid AF therapy using the EPi-Sense system compared to endocardial catheter ablation alone. • Hybrid AF therapy showed a 29% absolute improvement in efficacy at 12 months and a 35% absolute improvement at 18 months compared to catheter ablation. • The EPi-Sense system improves electrophysiology lab efficiency by reducing endocardial ablation times by over 40 minutes, enhancing patient throughput.

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