Patient Guide: The Long-term Safety and Effectiveness Evaluation of the QDOT MICRO System Use in Conjunction With VISITAG SURPOINT Module for the Treatment of Symptomatic Drug Refractory Paroxysmal Atrial Fibrillation.

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 21 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06324201
Status: 🟢 Enrolling Now
Condition: Paroxysmal Atrial Fibrillation
Phase: Not Specified

Where You Can Participate

This study is available at 21 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Mobile, Alabama
  • • Ventura, California
  • • And 18 more locations

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The Long-term Safety and Effectiveness Evaluation of the QDOT MICRO System Use in Conjunction With VISITAG SURPOINT Module for the Treatment of Symptomatic Drug Refractory Paroxysmal Atrial Fibrillation. - Join Clinical Trial NCTNCT06324201

How to Join This Clinical Trial - NCTNCT06324201

Learn how to participate in this Not Specified trial studying an investigational therapy for Paroxysmal 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. 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
Treatment Being Tested
Investigational treatment
Study Phase
Not Specified - Research study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT06324201 - 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 21 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35209 - United States

Status: RECRUITING

Clinical Research Site

Mobile, Alabama 36608 - United States

Status: RECRUITING

Clinical Research Site

Ventura, California 93003 - United States

Status: RECRUITING

Clinical Research Site

Aurora, Colorado 80012 - United States

Status: RECRUITING

Clinical Research Site

Naples, Florida 34102 - United States

Status: WITHDRAWN

Clinical Research Site

Sarasota, Florida 34239 - United States

Status: RECRUITING

Clinical Research Site

Atlanta, Georgia 30309 - United States

Status: RECRUITING

Clinical Research Site

Louisville, Kentucky 40205 - United States

Status: RECRUITING

Clinical Research Site

Boston, Massachusetts 02115 - United States

Status: NOT_YET_RECRUITING

Clinical Research Site

Lansing, Michigan 48912 - United States

Status: RECRUITING

And 11 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this Not Specified clinical trial for Paroxysmal 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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