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NCT06772493 · ClinicalTrials.gov registry record

ViewFlex X ICE First-in-Human Study

A clinical trial of Cardiac Arrhythmias, sponsored by Abbott Medical Devices.

Recruiting
Registry status
500
Enrollment target
7
Study locations

NCT06772493: Recruiting study of Cardiac Arrhythmias, sponsored by Abbott Medical Devices.

NCT06772493 is a study of Cardiac Arrhythmias that is actively recruiting participants, run by Abbott Medical Devices. The registered enrollment target is 500 participants, above the 442-participant average among 5 other Cardiac Arrhythmias trials with a reported enrollment target (13% higher). The trial reports 7 study locations across 7 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06772493, a study of Cardiac Arrhythmias, is actively recruiting participants, sponsored by Abbott Medical Devices.

RECRUITING
Registry status
500 participants
Enrollment target
7
Study locations

Study 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).

Conditions Studied

Interventions

  • DEVICE ViewFlex X ICE System

Study Locations (7)

Arkansas

  • St. Bernards Medical Center - Jonesboro

California

  • University of California, San Diego - La Jolla

Missouri

  • Research Medical Center - Kansas City

New York

  • NYU Langone Health - New York

Pennsylvania

  • Hospital of the University of Pennsylvania - Philadelphia

South Carolina

  • Medical University of South Carolina - Charleston

Texas

  • Houston Methodist Hospital - Houston

Trial Details

FieldValue
Enrollment Target 500 participants
Start Date 2024-12-16
Est. Completion 2026-06
Abbott Medical Devices

261 total trials

What NCT06772493 shows while recruiting

NCT06772493 is an observational study that tracks outcomes without assigning an intervention. The registered 500 participants enrollment target is mid-sized for trials with a published cap, above the 442-participant average among 5 other Cardiac Arrhythmias trials with a reported enrollment target (13% higher).

The record links to 1 condition, with Cardiac Arrhythmias appearing as the primary indexed condition, and to 1 intervention - of which ViewFlex X ICE System is the first listed.

NCT06772493 lists 7 locations in 7 states (Arkansas, California, Missouri).

Frequently Asked Questions

What is clinical trial NCT06772493 about?

NCT06772493 is a clinical study titled "ViewFlex X ICE First-in-Human Study". 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 Vie...

What is the current status of trial NCT06772493?

This trial is currently recruiting. The enrollment target is 500 participants. The study started on 2024-12-16. Estimated completion is 2026-06.

What conditions does trial NCT06772493 study?

This clinical trial studies the following conditions: Cardiac Arrhythmias.

What interventions are being tested in trial NCT06772493?

The interventions under investigation include: ViewFlex X ICE System (DEVICE).

Who is sponsoring clinical trial NCT06772493?

This trial is sponsored by Abbott Medical Devices, which has 261 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06772493 being conducted?

This trial has 7 study locations across Arkansas, California, Missouri, New York, Pennsylvania. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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Source: ClinicalTrials.gov NCT06772493, the US trial registry maintained by the National Library of Medicine. NCT06772493 (mid enrollment · multi site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.