Cleveland, OHNCT03355456Now EnrollingIRB Ready

Atrial Fibrillation - Symptomatic Clinical Trial in Cleveland, OH

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

Sponsored by Ohad Ziv

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Expert Care in Cleveland

Access atrial fibrillation - symptomatic specialists at no cost

IRB Approved

This study follows strict safety protocols and ethical guidelines

No-Cost Care

All study-related atrial fibrillation - symptomatic treatment provided free

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Check if you qualify for this atrial fibrillation - symptomatic clinical trial in Cleveland, OH

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Why Participate?

  • No-Cost Study Care

  • Local to Cleveland

    Convenient for OH 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 Cleveland site if eligible
  4. 4Begin participation

About This Atrial Fibrillation - Symptomatic Study in Cleveland

A two-pronged approach to evaluate long term success of non-paroxysmal ablation when using a: 1. specified low voltage-directed with pulmonary vein isolation (LD+PVI) approach compared to , 2. an approach of pulmonary vein isolation (PVI) alone.

Sponsor: Ohad Ziv

Who Can Participate

Inclusion Criteria

Subjects must meet all of the following criteria:
Non-Paroxysmal Atrial Fibrillation.
Failed or intolerable to at least 1 one antiarrhythmic drug (AAD).
18-85 year of age at time of consent.
Scheduled to undergo a clinically indicated AF ablation procedure.
Able and willing to comply with all protocol visit requirements.
Signed Patient Informed Consent (ICF).
Presence of low voltage in the left atrium on 3-D map during index catheter ablation procedure

Exclusion Criteria

Subjects will be excluded if any of the follow criteria are present:
History of prior left-sided catheter or surgical ablation for AF or atypical atrial flutter, including MAZE or mini MAZE.
Prior ablation for typical atrial flutter or left-sided ablation for WPW, AV node reentry tachycardia or focal ectopic atrial tachycardia may be included.
Uncontrolled heart Failure or NYHA Class IIIb or IV heart failure.
Ejection Fraction \< 0.20.
Active ventricular tachycardia requiring treatment with catheter ablation or anti-arrhythmic drug within the last 6 months.
Left atrial size \> 60 mm diameter on echocardiogram.
"Long standing" persistent AF defined as \> or = 1 year of continuous atrial fibrillation at the time of enrollment.
Severe pulmonary hypertension (PAP \> 70 mmHg)
Unstable valvular disease.
AF secondary to electrolyte imbalance, thyroid disease or reversible non- cardiac cause.
Poor candidate for general anesthesia.
Anticipated survival \< 1 year.
MI or CABG within 3 months.
Left atrial thrombus in pre-procedure imaging within 4 weeks of the ablation procedure.
Any documented thromboembolic event within 6 months of the ablation procedure.
Contraindication to anticoagulation.
Inability to have implantable monitoring device for atrial fibrillation burden with no pre-existing cardiac device that can monitor atrial arrhythmias OR inability to wear external Holter Monitor continuously for 4 weeks.
Significant congenital anomaly or medical condition that may affect the integrity of study data.
Women who are pregnant - pregnancy test required if pre-menopausal or non-sterile.
Active enrollment in another investigational study involving a drug or device.
Inability to undergo complete voltage mapping in normal sinus rhythm - see intraprocedural protocol.
Presence of any medical or psychological condition or medical non-compliance history that may adversely impact study outcomes.

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 Cleveland?

Yes, this clinical trial (NCT03355456) has an active research site in Cleveland, OH 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 - Symptomatic Treatment Options in Cleveland, OH

If you're searching for atrial fibrillation - symptomatic treatment options in Cleveland, OH, this clinical trial (NCT03355456) 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 Cleveland research site is actively enrolling participants for this clinical trial. You'll receive care from experienced atrial fibrillation - symptomatic 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 - symptomatic clinical trials near you to find additional studies recruiting in your area.

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