Bloomington, INNCT06027788Now EnrollingIRB Ready

Delirium Clinical Trial in Bloomington, IN

Access cutting-edge delirium treatment through this clinical trial at a research site in Bloomington. Study-provided care at no cost to qualified participants.

Sponsored by Icahn School of Medicine at Mount Sinai

Quick Self-Assessment

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Expert Care in Bloomington

Access delirium specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related delirium treatment provided free

Apply for This Bloomington Location

Check if you qualify for this delirium clinical trial in Bloomington, IN

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Your information is protected and will only be shared with the research team.

Why Participate?

  • No-Cost Study Care

  • Local to Bloomington

    Convenient for IN residents

  • Cutting-Edge Treatment

    Access to innovative therapies

  • Expert Medical Care

    Close monitoring by specialists

  • Possible Compensation*

    For time and travel

*Compensation varies by study. Confirm details with coordinator.

Simple Process

  1. 1Submit this form
  2. 2Phone screening
  3. 3Visit Bloomington site if eligible
  4. 4Begin participation

About This Delirium Study in Bloomington

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

Sponsor: Icahn School of Medicine at Mount Sinai

Who Can Participate

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

Not sure if you qualify? Submit your interest and a study coordinator will help determine your eligibility.

Frequently Asked Questions

Q:Is this study available in Bloomington?

Yes, this clinical trial (NCT06027788) has an active research site in Bloomington, IN that is currently enrolling participants.

Q:Is it safe to participate?

Clinical trials follow strict safety guidelines and ethical standards. This study has been reviewed and approved, and participants are closely monitored by medical professionals. You can withdraw at any time.

Q:Will I be compensated?

Many clinical trials offer compensation for your time and travel expenses. Specific compensation details will be discussed during the screening process. All study-related medical care is provided at no cost.

Q:Can I leave the trial if I change my mind?

Absolutely. Participation is completely voluntary. You have the right to withdraw from the study at any time, for any reason, without penalty.

Still have questions? Our study coordinators are here to help.

Delirium Treatment Options in Bloomington, IN

If you're searching for delirium treatment options in Bloomington, IN, this clinical trial (NCT06027788) may be an excellent opportunity. Clinical trials provide access to cutting-edge treatments that aren't yet available to the general public, often at no cost to participants.

Our Bloomington research site is actively enrolling participants for this clinical trial. You'll receive care from experienced delirium specialists who are at the forefront of medical research. All study-related care, including examinations, treatments, and monitoring, is provided at no cost to qualified participants.

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Secure · Expert Care · Bloomington, IN