Naples, FLNCT06529978Now EnrollingIRB Ready

Persistent Atrial Fibrillation Clinical Trial in Naples, FL

Access cutting-edge persistent atrial fibrillation treatment through this clinical trial at a research site in Naples. Study-provided care at no cost to qualified participants.

Sponsored by CoreMap Inc.

Quick Self-Assessment

See if you qualify for this Naples location

Preparing your pre-screening questions…

Expert Care in Naples

Access persistent atrial fibrillation specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related persistent atrial fibrillation treatment provided free

Apply for This Naples Location

Check if you qualify for this persistent atrial fibrillation clinical trial in Naples, FL

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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 Naples

    Convenient for FL 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 Naples site if eligible
  4. 4Begin participation

About This Persistent Atrial Fibrillation Study in Naples

This is a global, multi-site, prospective, feasibility study.

Sponsor: CoreMap Inc.

Who Can Participate

Inclusion Criteria

Subject has persistent or long-standing persistent AF, at the discretion of the investigator (Phase 1 \& 2)
Subject has PerAF with no history of prior AF ablation therapy (Phase 3)
Subject is 18 to 80 years of age
Subject has presence of AF-related symptoms and is scheduled for clinically indicated standard of care AF ablation to manage PerAF (Phase 2 or 3) or long-standing PerAF (Phase 2)
Subject is able to provide written informed consent
Subject is able and willing to complete all study procedures

Exclusion Criteria

Any of the following within three months of enrollment:
Myocardial infarction (MI)
Any surgical or percutaneous cardiac procedure including coronary intervention and cardiac ablation
Confirmed thrombus on imaging
Any of the following within six months of enrollment:
Cardiac surgery including coronary artery bypass grafting, ventriculotomy, atriotomy
Thromboembolic event (stroke)
Any of the following cardiac conditions:
New York Heart Association (NYHA) IV
Left ventricular ejection fraction (LVEF) \< 30%
Left atrial diameter \>55mm (anterioposterior) (Phase 3)
Carotid stenting or endarterectomy
Atrial or ventricular septal closure or left atrial appendage closure
Implanted permanent pacemaker, biventricular pacemaker, or any type of implantable cardiac defibrillator; loop recorders are permitted.
Presence of intramural thrombus, tumor (including atrial myxoma), or other abnormality that precludes vascular access, catheter introduction, or manipulation
Unstable angina
Prior mitral or tricuspid valve surgery, repair, prosthetic or mechanical valve
Moderate to severe mitral valve stenosis or other severe valvular disease
Any blood clotting or bleeding abnormalities
Contraindication to systemic anticoagulation
AF secondary to electrolyte imbalance, acute alcohol intoxication, or reversible or non-cardiac cause
Body mass index (BMI) \> 40 kg/m2
Severe pulmonary disease, pulmonary hypertension, or any chronic respiratory condition
Renal failure requiring dialysis or transplant
Acute illness, active systemic infection, or sepsis
Active drug or alcohol dependency
Hypertrophic cardiomyopathy or cardiac amyloidosis
Cor pulmonale
Any contra-indication that may extend procedure time, at the discretion of the operator
Any woman known to be pregnant or breastfeeding, or any woman of childbearing potential who is not on a reliable form of birth regulation method or abstinence
Subject considered part of vulnerable population
Life expectancy less than one year
Employee of the study site or Sponsor
Subjects who are currently enrolled in another study that would directly interfere with this study

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 Naples?

Yes, this clinical trial (NCT06529978) has an active research site in Naples, FL 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.

Persistent Atrial Fibrillation Treatment Options in Naples, FL

If you're searching for persistent atrial fibrillation treatment options in Naples, FL, this clinical trial (NCT06529978) 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 Naples research site is actively enrolling participants for this clinical trial. You'll receive care from experienced persistent atrial fibrillation 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 persistent atrial fibrillation clinical trials near you to find additional studies recruiting in your area.

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Secure · Expert Care · Naples, FL