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NCT06203054 · ClinicalTrials.gov registry record · NA

CLIP-IT Post-Market Study

A NA study of Left Atrial Appendage Exclusion, sponsored by Medtronic Cardiac Surgery.

Active
Registry status
NA
Development phase
150
Enrollment target
15
Study locations

NCT06203054 is a NA study of Left Atrial Appendage Exclusion that is active but no longer recruiting, run by Medtronic Cardiac Surgery. The registered enrollment target is 150 participants. The trial reports 15 study locations across 11 states.

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The verdict

NCT06203054, a NA study of Left Atrial Appendage Exclusion, is active but no longer recruiting, sponsored by Medtronic Cardiac Surgery.

ACTIVE NOT RECRUITING
Registry status
NA
Development phase
150 participants
Enrollment target
15
Study locations

Study Summary

The purpose of this study is to collect post-market clinical evidence on performance and clinical outcomes of the Penditure™ Left Atrial Appendage (LAA) Exclusion System in subjects undergoing concomitant cardiac surgery.

Interventions

  • DEVICE Penditure™ Left Atrial Appendage (LAA) Exclusion System

Study Locations (15)

Pennsylvania

  • UPMC Pinnacle Harrisburg Campus - Harrisburg
  • University of Pittsburgh Medical Center UPMC Presbyterian - Pittsburgh
  • Lankenau Institute for Medical Research - Wynnewood

Michigan

  • University of Michigan Health System - Ann Arbor
  • Corewell Health - Grand Rapids

Ohio

  • University Hospitals Cleveland Medical Center - Cleveland
  • ProMedica Toledo Hospital - Toledo

Georgia

  • Emory Saint Joseph's Hospital - Atlanta

Illinois

  • Northwestern Memorial Hospital - Chicago

Indiana

  • Ascension St. Vincent Heart Center - Carmel

Minnesota

  • Mayo Clinic Saint Marys Campus - Rochester

Missouri

  • Barnes Jewish Hospital - St Louis

Trial Details

FieldValue
Enrollment Target 150 participants
Start Date 2024-02-26
Est. Completion 2029-02
Phase NA

Sponsor

Medtronic Cardiac Surgery

7 total trials

What the Registry Record Tells You About NCT06203054

The ClinicalTrials.gov registry entry for NCT06203054 describes a study currently listed as active not recruiting, categorized as NA. The registered enrollment target is 150 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Medtronic Cardiac Surgery, which has 7 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Left Atrial Appendage Exclusion appearing as the primary indexed condition, and to 1 intervention - of which Penditure™ Left Atrial Appendage (LAA) Exclusion System is the first listed.

NCT06203054 reports 15 study locations spanning 11 distinct geographic areas - top geographies include Pennsylvania, Michigan, Ohio.

Frequently Asked Questions

What is clinical trial NCT06203054 about?

NCT06203054 is a clinical study titled "CLIP-IT Post-Market Study". The purpose of this study is to collect post-market clinical evidence on performance and clinical outcomes of the Penditure™ Left Atrial Appendage (LAA) Exclusion System in subjects undergoing concomitant cardiac surgery.

What is the current status of trial NCT06203054?

This trial is currently active not recruiting. It is a NA study. The enrollment target is 150 participants. The study started on 2024-02-26. Estimated completion is 2029-02.

What conditions does trial NCT06203054 study?

This clinical trial studies the following conditions: Left Atrial Appendage Exclusion.

What interventions are being tested in trial NCT06203054?

The interventions under investigation include: Penditure™ Left Atrial Appendage (LAA) Exclusion System (DEVICE).

Who is sponsoring clinical trial NCT06203054?

This trial is sponsored by Medtronic Cardiac Surgery, which has 7 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06203054 being conducted?

This trial has 15 study locations across Georgia, Illinois, Indiana, Michigan, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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.