Actively Recruiting
Intracardiac Echocardiography Guided Watchman Device Implant
Led by The Cleveland Clinic · Updated on 2025-10-21
100
Participants Needed
1
Research Sites
265 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
This study is to look at the success of Intracardiac Echocardiography (ICE) in the Watchman procedure. Currently the process is to use a Transesophageal Echocardiography (TEE) to place the Watchman in patients. This study is aiming to show how the ICE is just as effective in placing the device correctly and effectively.
CONDITIONS
Official Title
Intracardiac Echocardiography Guided Watchman Device Implant
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients must meet guideline-established criteria for Watchman device implant
- Patients must not be enrolled in any active clinical trial
You will not qualify if you...
- Patients who cannot undergo procedural TEE and require ICE-only implant
- Patients receiving a concomitant ablation procedure
- Patients with prior incomplete surgical or percutaneous left atrial appendage ligation or exclusion
- Patients with anticipated difficulty delivering trans-septal equipment due to devices like PFO or ASD closure
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 1 location
1
Cleveland Clinic
Cleveland, Ohio, United States, 44195
Actively Recruiting
Research Team
O
Oussama Wazni, MD
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
DIAGNOSTIC
Number of Arms
1
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