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NCT07098858 · ClinicalTrials.gov registry record

The WiSE®-UP Registry (The WiSE System Utilization & Performance Registry)

A clinical trial of Heart Failure, sponsored by EBR Systems.

Recruiting
Registry status
320
Enrollment target
5
Study locations

NCT07098858: Recruiting study of Heart Failure, sponsored by EBR Systems.

NCT07098858 is a study of Heart Failure that is actively recruiting participants, run by EBR Systems. The registered enrollment target is 320 participants, below the 2,048-participant average among 397 other Heart Failure trials with a reported enrollment target (84% lower). The trial reports 5 study locations across 5 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT07098858, a study of Heart Failure, is actively recruiting participants, sponsored by EBR Systems.

RECRUITING
Registry status
320 participants
Enrollment target
5
Study locations

Study Summary

Observe to understand product performance, including patient safety, clinical outcomes, and CRT response information associated with the use of the market-released WiSE System

Conditions Studied

Interventions

  • DEVICE The Wise System

Study Locations (5)

Arkansas

  • Arrhythmia Research Group (St. Bernards Hospital) - Jonesboro

Florida

  • Naples Community Hospital - Naples

Michigan

  • University of Michigan - Ann Arbor

New York

  • Weill Cornell Medicine - New York

Pennsylvania

  • Penn State Health - Hershey

Trial Details

FieldValue
Enrollment Target 320 participants
Start Date 2025-11-03
Est. Completion 2032-09-30

Sponsor

EBR Systems

2 total trials

What the Registry Record Tells You About NCT07098858

The ClinicalTrials.gov registry entry for NCT07098858 describes a study currently listed as recruiting, categorized as an unspecified phase. The registered enrollment target is 320 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,048-participant average among 397 other Heart Failure trials with a reported enrollment target (84% lower). The listed sponsor is EBR Systems, which has 2 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Heart Failure appearing as the primary indexed condition, and to 1 intervention - of which The Wise System is the first listed.

NCT07098858 reports 5 study locations spanning 5 distinct geographic areas - top geographies include Arkansas, Florida, Michigan.

Frequently Asked Questions

What is clinical trial NCT07098858 about?

NCT07098858 is a clinical study titled "The WiSE®-UP Registry (The WiSE System Utilization & Performance Registry)". Observe to understand product performance, including patient safety, clinical outcomes, and CRT response information associated with the use of the market-released WiSE System

What is the current status of trial NCT07098858?

This trial is currently recruiting. The enrollment target is 320 participants. The study started on 2025-11-03. Estimated completion is 2032-09-30.

What conditions does trial NCT07098858 study?

This clinical trial studies the following conditions: Heart Failure.

What interventions are being tested in trial NCT07098858?

The interventions under investigation include: The Wise System (DEVICE).

Who is sponsoring clinical trial NCT07098858?

This trial is sponsored by EBR Systems, which has 2 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT07098858 being conducted?

This trial has 5 study locations across Arkansas, Florida, Michigan, 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

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, the data changelog, or report a data error.