Clinical Trial

ViewFlex X ICE First-in-Human Study

Study acronym: ViewFlex X FIH
Recruiting
View on ClinicalTrials.gov →
Summary
This prospective, acute, first-in-human, non-significant risk study is intended to evaluate a modified version of the ViewFlex X ICE Catheter, Sensor Enabled (ViewFlex X SE) and ViewMate Multi Ultrasound Console (VMM) ICE data integration with the EnSite X EP System (hereafter referred to as the ViewFlex X ICE System).
Protocol Amendment History 3 amendments
This ClinicalTrials.gov record has been amended 3 times since 2025-01-10; most recent amendment 2026-05-30.
Trial Details
NCT Number NCT06772493
Lead Sponsor Abbott Medical Devices
Conditions Cardiac Arrhythmias
Enrollment 500 participants
Start Date 2024-12-16
Primary Completion 2026-06 (estimated)
Study Completion 2026-06 (estimated)
Updated on ClinicalTrials.gov 2026-06-02