Patient Guide: Safety and Effectiveness of the Globe® Pulsed Field System for Treating Patients With Symptomatic Paroxysmal or Persistent Atrial Fibrillation

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 19 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05462145
Status: 🟢 Enrolling Now
Condition: Paroxysmal Atrial Fibrillation, Persistent Atrial Fibrillation
Phase: NA

Where You Can Participate

This study is available at 19 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Birmingham, Alabama
  • • Jonesboro, Arkansas
  • • And 16 more locations

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Safety and Effectiveness of the Globe® Pulsed Field System for Treating Patients With Symptomatic Paroxysmal or Persistent Atrial Fibrillation - Join Clinical Trial NCTNCT05462145

How to Join This Clinical Trial - NCTNCT05462145

Learn how to participate in this NA trial studying an investigational therapy for Paroxysmal Atrial Fibrillation, Persistent Atrial Fibrillation. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Paroxysmal Atrial Fibrillation, Persistent Atrial Fibrillation. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Paroxysmal Atrial Fibrillation, Persistent Atrial Fibrillation
Treatment Being Tested
Investigational treatment
Study Phase
NA - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05462145 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 19 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35233 - United States

Status: WITHDRAWN

Clinical Research Site

Birmingham, Alabama 35243 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Jonesboro, Arkansas 72401 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

San Francisco, California 94109 - United States

Status: RECRUITING

Clinical Research Site

Jacksonville, Florida 32204 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Miami, Florida 33133 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Baltimore, Maryland 21287 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

Boston, Massachusetts 02114 - United States

Status: WITHDRAWN

Clinical Research Site

Royal Oak, Michigan 48073 - United States

Status: ACTIVE_NOT_RECRUITING

Clinical Research Site

New York, New York 10029 - United States

Status: ACTIVE_NOT_RECRUITING

And 9 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this NA clinical trial for Paroxysmal Atrial Fibrillation, Persistent Atrial Fibrillation:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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