Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

RECRUITING

Medtronic Cardiac Surgery PMCF Registry

NCT04073420 · View on ClinicalTrials.gov ↗

Study Summary

This registry is being conducted to support ongoing post-market surveillance activities.

Conditions Studied

Interventions

  • DEVICE Surgical Heart Valve Repair Products
  • DEVICE Surgical Heart Valve Replacement Products

Study Locations (20)

Other

  • Allgemeines Krankenhaus - Universitätskliniken Wien — Vienna
  • UZ Leuven — Leuven
  • Hôpital Haut-Lévêque - CHU de Bordeaux — Pessac
  • Schüchtermann-Klinik — Bad Rothenfelde
  • Herzzentrum Dresden GmbH Universitätsklinik — Dresden
  • Universitätsklinikum Düsseldorf — Düsseldorf
  • Albertinen-Herz- und Gefäßzentrum — Hamburg
  • Herzzentrum Leipzig — Leipzig
  • Deutsches Herzzentrum München Klinik an der TU München — München

New York

  • Mount Sinai Medical Center — New York
  • Saint Francis Hospital — Roslyn
  • Saint Josephs Hospital Health Center — Syracuse

Texas

  • Baylor St. Luke's Medical Center — Houston
  • The Heart Hospital Plano — Plano

Georgia

  • WellStar Kennestone Hospital — Marietta

Michigan

  • University of Michigan — Ann Arbor

North Carolina

  • Duke University Medical Center — Durham

Ohio

  • University Hospitals Cleveland — Cleveland

Pennsylvania

  • University of Pittsburgh Medical Center UPMC Presbyterian — Pittsburgh

Trial Details

FieldValue
Enrollment Target 2,700 participants
Start Date 2019-12-02
Est. Completion 2039-12-31

Sponsor

Medtronic Cardiac Surgery

7 total trials

Interested in This Trial?

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT04073420

The ClinicalTrials.gov registry entry for NCT04073420 describes a study currently listed as recruiting. It is categorized as an unspecified phase, 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 2,700 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 Valve Disease, Heart appearing as the primary indexed condition, and to 2 interventions — of which Surgical Heart Valve Repair Products 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: NCT04073420 reports 20 study locations spanning 9 distinct geographic areas — top geographies include Other, New York, Texas. 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 NCT04073420 about?

NCT04073420 is a clinical study titled "Medtronic Cardiac Surgery PMCF Registry". This registry is being conducted to support ongoing post-market surveillance activities.

What is the current status of trial NCT04073420?

This trial is currently recruiting. The enrollment target is 2,700 participants. The study started on 2019-12-02. Estimated completion is 2039-12-31.

What conditions does trial NCT04073420 study?

This clinical trial studies the following conditions: Valve Disease, Heart. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT04073420?

The interventions under investigation include: Surgical Heart Valve Repair Products (DEVICE), Surgical Heart Valve Replacement Products (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT04073420?

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 NCT04073420 being conducted?

This trial has 20 study locations across Georgia, Michigan, New York, North Carolina, Ohio. 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