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NCT06702501 · ClinicalTrials.gov registry record · NA

The PeriCut Catheter System Early Feasibility Study (REIMAGINE-HFpEF)

A NA study of Heart Failure With Preserved Ejection Fraction, sponsored by Heart Failure Solutions.

Recruiting
Registry status
NA
Development phase
10
Enrollment target
1
Study location

NCT06702501 is a NA study of Heart Failure With Preserved Ejection Fraction that is actively recruiting participants, run by Heart Failure Solutions. The registered enrollment target is 10 participants, below the 2,288-participant average among 42 other Heart Failure With Preserved Ejection Fraction trials with a reported enrollment target (100% lower). The trial reports 1 study location across 1 state.

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The verdict

NCT06702501, a NA study of Heart Failure With Preserved Ejection Fraction, is actively recruiting participants, sponsored by Heart Failure Solutions.

RECRUITING
Registry status
NA
Development phase
10 participants
Enrollment target
1
Study location

Study Summary

The PeriCut early feasibility study will evaluate the safety and feasibility of successfully performing a minimally invasive pericardiotomy in patients with heart failure with preserved ejection fraction using the PeriCut Catheter System.

Conditions Studied

Heart Failure With Preserved Ejection Fraction

Interventions

  • DEVICE PeriCut Catheter System performs minimally invasive pericardiotomy

Study Locations (1)

Minnesota

  • Mayo Clinic - Rochester

Trial Details

FieldValue
Enrollment Target 10 participants
Start Date 2025-02-17
Est. Completion 2026-06-01
Phase NA

Sponsor

Heart Failure Solutions

1 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06702501

The ClinicalTrials.gov registry entry for NCT06702501 describes a study currently listed as recruiting, categorized as NA. The registered enrollment target is 10 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 2,288-participant average among 42 other Heart Failure With Preserved Ejection Fraction trials with a reported enrollment target (100% lower). The listed sponsor is Heart Failure Solutions, which has 1 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Heart Failure With Preserved Ejection Fraction appearing as the primary indexed condition, and to 1 intervention - of which PeriCut Catheter System performs minimally invasive pericardiotomy is the first listed.

NCT06702501 reports 1 study location spanning 1 distinct geographic area - top geographies include Minnesota.

Frequently Asked Questions

What is clinical trial NCT06702501 about?

NCT06702501 is a clinical study titled "The PeriCut Catheter System Early Feasibility Study (REIMAGINE-HFpEF)". The PeriCut early feasibility study will evaluate the safety and feasibility of successfully performing a minimally invasive pericardiotomy in patients with heart failure with preserved ejection fraction using the PeriCut Catheter System.

What is the current status of trial NCT06702501?

This trial is currently recruiting. It is a NA study. The enrollment target is 10 participants. The study started on 2025-02-17. Estimated completion is 2026-06-01.

What conditions does trial NCT06702501 study?

This clinical trial studies the following conditions: Heart Failure With Preserved Ejection Fraction.

What interventions are being tested in trial NCT06702501?

The interventions under investigation include: PeriCut Catheter System performs minimally invasive pericardiotomy (DEVICE).

Who is sponsoring clinical trial NCT06702501?

This trial is sponsored by Heart Failure Solutions, which has 1 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06702501 being conducted?

This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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