At a glance
ClinicalIndex Comparison RecordN/ACompleted· 100 enrolled
Drug / intervention
intra-procedural intracardiac echocardiography (ICE) probedevice
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.
Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.
Safety and Feasibility of Intra-Cardiac Echocardiography in Guiding Left Atrial Appendage Occlusion With the Watchman Device: The ICE WATCHMAN Study
In Brief
A clinical study evaluating intra-procedural intracardiac echocardiography (ICE) probe for Left Atrial Appendage Occlusion. Completed, enrolled 100 participants across 2 sites.
Detailed Summary
The purpose of this research is to to assess the feasibility and safety of left atrial appendage (LAA) occlusion with the WATCHMAN FLX™ device using a standardized intra-procedural intracardiac echocardiography (ICE) protocol under moderate sedation for procedural guidance.
Study Details
Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
ConditionsLeft Atrial Appendage Occlusion
CountriesUnited States
Collaborators--
Timeline
N/ACompletedFinished
20222023202420252026
First PostedNov 2021
Enrollment StartJan 2022
Primary CompletionDec 2023
TodayJul 2026
First PostedNov 29, 2021
Enrollment StartJan 4, 2022
Primary CompletionDec 15, 2023
TodayJul 2, 2026
Enrollment to primary: 1.9 yearsPosted 4.6 years ago
Interventions
intra-procedural intracardiac echocardiography (ICE) probedevice
placing the WATCHMAN FLX device using the intra-procedural intracardiac echocardiography (ICE) probe.