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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 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.

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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

Cardiac Arrhythmias

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

Sponsor

Abbott Medical Devices

261 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06772493

The ClinicalTrials.gov registry entry for NCT06772493 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 500 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 442-participant average among 5 other Cardiac Arrhythmias trials with a reported enrollment target (13% higher). The listed sponsor is Abbott Medical Devices, which has 261 total studies on file at ClinicalTrials.gov.

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 reports 7 study locations spanning 7 distinct geographic areas - top geographies include 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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Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.