Bay Shore, NYNCT07620262Now EnrollingIRB Ready

Atrial Fibrillation (AF) Clinical Trial in Bay Shore, NY

Access cutting-edge atrial fibrillation (af) treatment through this clinical trial at a research site in Bay Shore. Study-provided care at no cost to qualified participants.

Sponsored by Northwell Health

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Expert Care in Bay Shore

Access atrial fibrillation (af) specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related atrial fibrillation (af) treatment provided free

Apply for This Bay Shore Location

Check if you qualify for this atrial fibrillation (af) clinical trial in Bay Shore, NY

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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 Bay Shore

    Convenient for NY 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 Bay Shore site if eligible
  4. 4Begin participation

About This Atrial Fibrillation (AF) Study in Bay Shore

This is a single-arm, open label, clinical outcome study to research the durability (success) of receiving a pulsed field ablation (PFA) per standard of care for treatment of atrial fibrillation during a subsequent procedure for the insertion of a left atrial appendage occlusion (LAAO) device. The reassessment of the initial ablation will be performed with or without additional ablation if needed.

Sponsor: Northwell Health

Who Can Participate

Inclusion Criteria

Participant is ≥ 18 years of age, or older if specified by local law
Participant has documented paroxysmal or persistent atrial fibrillation not related to a reversible cause
Participant has AF-related symptoms, and/or presence of CHF or LV dysfunction
Participant has a CHADSVASc\>=3
There is appropriate rationale to seek a non-pharmacologic alternative to long-term oral anticoagulation for thromboembolic protection
Participant is willing and capable of providing informed consent
Participant is willing and capable of participating in all testing associated with this clinical investigation at an approved clinical investigational center

Exclusion Criteria

Participant has had prior AF ablation (including surgical ablation)
Participant has had prior left atrial appendage occlusion or closure
Participant has an intracardiac mass or thrombus
Participant has had a bleeding disorder or inability to tolerate short-term oral anticoagulation
Participant has a life expectancy \< 1 year
Participant has had recent MI, CVA, or cardiac surgery in preceding 90 days
Participant has an inability to comply with outpatient follow-up, or cognitive impairment that precludes understanding of procedure risks and benefits Participant has an active systemic infection
Participant has a mechanical heart valve through which the catheter must pass, or severe mitral stenosis
Participant has a vena cava embolic protection filter devices and/or known femoral thrombus who require catheter insertion from the femoral approach
Participant had congenital heart disease where the underlying abnormality increases the risk of ablation (e.g. severe rotational anomalies of the heart or great vessels)
Participant is woman of childbearing potential who is pregnant, lactating, not using a reliable form of contraception, or who is planning to become pregnant during the anticipated study period

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 Bay Shore?

Yes, this clinical trial (NCT07620262) has an active research site in Bay Shore, NY 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.

Atrial Fibrillation (AF) Treatment Options in Bay Shore, NY

If you're searching for atrial fibrillation (af) treatment options in Bay Shore, NY, this clinical trial (NCT07620262) 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 Bay Shore research site is actively enrolling participants for this clinical trial. You'll receive care from experienced atrial fibrillation (af) 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.

Looking for more options? Browse all atrial fibrillation (af) clinical trials near you to find additional studies recruiting in your area.

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See all atrial fibrillation clinical trials recruiting in Bay Shore — not just this study.

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Secure · Expert Care · Bay Shore, NY