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RECRUITING NA

CTSN Embolic Protection Trial

NCT06027788 · View on ClinicalTrials.gov ↗

Study Summary

This is a prospective, multi-center, randomized effectiveness trial of the CardioGard Embolic Protection Cannula in high-risk valve surgery patients.

Interventions

  • DEVICE CardioGard Embolic Protection Cannula
  • DEVICE Standard Aortic Cannula

Study Locations (20)

New York

  • Columbia University Medical Center — New York
  • New York Presbyterian-Cornell Medical Center — New York
  • NYU Langone Hospital Brooklyn — New York
  • Northwell Health — New York
  • Montefiore Medical Center — The Bronx

Indiana

  • Indiana University — Bloomington
  • Indiana Ohio Heart — Fort Wayne

Maryland

  • Johns Hopkins Medicine — Baltimore
  • University of Maryland — College Park

Arkansas

  • CHI St. Vincent Heart Institute — North Little Rock

California

  • Keck Hospital of the University of Southern California — Los Angeles

Georgia

  • Emory University — Atlanta

Louisiana

  • Ochsner Clinic — New Orleans

Maine

  • Maine Medical Center — Portland

Trial Details

FieldValue
Enrollment Target 842 participants
Start Date 2023-09-18
Est. Completion 2027-04-01
Phase NA

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT06027788

The ClinicalTrials.gov registry entry for NCT06027788 describes a study currently listed as 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 842 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Icahn School of Medicine at Mount Sinai, which has 946 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.

The record links to 5 conditions, with Coronary Artery Disease appearing as the primary indexed condition, and to 2 interventions — of which CardioGard Embolic Protection Cannula 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: NCT06027788 reports 20 study locations spanning 14 distinct geographic areas — top geographies include New York, Indiana, Maryland. 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 NCT06027788 about?

NCT06027788 is a clinical study titled "CTSN Embolic Protection Trial". This is a prospective, multi-center, randomized effectiveness trial of the CardioGard Embolic Protection Cannula in high-risk valve surgery patients.

What is the current status of trial NCT06027788?

This trial is currently recruiting. It is a NA study. The enrollment target is 842 participants. The study started on 2023-09-18. Estimated completion is 2027-04-01.

What conditions does trial NCT06027788 study?

This clinical trial studies the following conditions: Coronary Artery Disease, Acute Kidney Injury, Ischemic Stroke, Delirium, Heart Valve Disease. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT06027788?

The interventions under investigation include: CardioGard Embolic Protection Cannula (DEVICE), Standard Aortic Cannula (DEVICE). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT06027788?

This trial is sponsored by Icahn School of Medicine at Mount Sinai, which has 946 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT06027788 being conducted?

This trial has 20 study locations across Arkansas, California, Georgia, Indiana, Louisiana. 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