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CTSN Embolic Protection Trial

Recruiting

Embolic Protection in Patients Undergoing High-Risk Valve Surgery

Who can join

Ages 60 and older · All sexes

Full eligibility criteria
Inclusion Criteria:

* Age ≥ 60 years
* Planned de novo or redo:

  * Surgical aortic valve replacement SAVR ± ascending aortic repair (if circulatory arrest is not required) ± CABG
  * Mitral valve replacement (MVR) ± CABG
  * Mitral Valve Repair + CABG,
  * Double/Triple valve surgery ± CABG; Ross procedure These procedures can be done via a full or minimal-access sternotomy (using central aortic perfusion cannulae) with legally marketed valve(s), and can be done in combination with an left atrial appendage (LAA) closure/excision or partial/complete Maze procedure.
  * Valve sparing aortic root replacement (David procedure)
  * Valve sparing aortic root replacement (David procedure)
* No evidence of neurological impairment as defined by a NIHSS ≤1 and modified Rankin scale (mRS) ≤2 within 30 days prior to randomization
* Ability to provide informed consent and comply with the protocol

Exclusion Criteria:

* History of clinical stroke within 3 months prior to randomization
* Cerebral and or aortic arch arteriography or interventions within 3 days of the planned procedure
* Coronary catheterization within 3 days of index procedure, and the required repeat NIHSS score post-catheterization is worse than the screening/baseline NIHSS score conducted prior to the catheterization
* Active endocarditis at time of randomization with vegetation criteria
* Clinical signs of cardiogenic shock or treatment with IV inotropic therapy prior to randomization
* Participation in an interventional (drug or device) trial
* Isolated mitral valve repair, isolated tricuspid valve repair or combined mitral valve repair and tricuspid valve repair
* Anticipated requirement for prolonged mechanical ventilation greater than 48 hours after surgery in the opinion of the investigator
* Planned concomitant carotid endarterectomy during index surgical procedure

About the study

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

What is being tested

Sponsor: Icahn School of Medicine at Mount Sinai · Participants: 842 · Started: Sep 18, 2023

Contact the study team

Official record on ClinicalTrials.gov — NCT06027788

Locations in the U.S.

ArkansasCHI St. Vincent Heart Institute, North Little Rock
CaliforniaKeck Hospital of the University of Southern California, Los Angeles
GeorgiaEmory University, Atlanta
LouisianaOchsner Clinic, New Orleans
MaineMaine Medical Center, Portland
MarylandJohns Hopkins Medicine, Baltimore
University of Maryland, College Park
MassachusettsMassachusetts General Hospital, Boston
MichiganUniversity of Michigan, Ann Arbor
MinnesotaMayo Clinic, Rochester
MissouriSaint Luke's Hospital of Kansas City, Kansas City
New YorkColumbia University Medical Center, New York
Northwell Health, New York
Montefiore Medical Center, The Bronx
North CarolinaDuke University, Durham
OhioUniversity of Cincinnati Medical Center, Cincinnati
Cleveland Clinic, Cleveland
PennsylvaniaHospital of the University of Pennsylvania, Philadelphia
VirginiaUniversity of Virginia, Charlottesville (Not yet recruiting)
West VirginiaWest Virginia University, Morgantown

Conditions

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.