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ACTIVE NOT RECRUITING NA

CLIP-IT Post-Market Study

NCT06203054 · View on ClinicalTrials.gov ↗

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

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06203054

The ClinicalTrials.gov registry entry for NCT06203054 describes a study currently listed as active not recruiting. It is categorized as NA, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. 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, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

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. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.

Geographic footprint matters for practical reasons: NCT06203054 reports 15 study locations spanning 11 distinct geographic areas — top geographies include Pennsylvania, Michigan, Ohio. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.

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. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06203054?

The interventions under investigation include: Penditure™ Left Atrial Appendage (LAA) Exclusion System (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06203054?

This trial is sponsored by Medtronic Cardiac Surgery, which has 7 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

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.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial