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NCT07651852Recruiting

Globe Registry: Globe® Pulsed Field System Registry Study for Treating Patients With Symptomatic Atrial Fibrillation

Source: ClinicalTrials.gov · Last updated 26 Oct 2026

Brief summary (registry, in English)

This post-market registry is designed to collect real world data on the use of the Globe PF System for the treatment of atrial fibrillation (AF).

Status (registry)
Recruiting
Study type
Observational
Enrollment
500 (estimated)
First submitted
11 Jun 2026
Start date
9 Oct 2026
Primary completion date
Oct 2029
Lead sponsor
Kardium Inc.
NCT number
NCT07651852

What you commit to

  • Study type: Observational
  • Planned participants: 500
  • From 9 Oct 2026 to the primary completion date, Oct 2029
  • 2 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Current enrollment in any investigational study of a medical device, biologic, or drug not pre-approved by Kardium

Other

  • Patients whose life expectancy is 1 year or less
  • Contraindication to left atrial catheter ablation or PF ablation

Who the study is looking for

  • Patients with a planned ablation procedure using the commercially available Globe PF System

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (2)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Overlake Hospital
Coordinator of this site? Confirm its status
BellevueUnited StatesRecruiting
Arrhythmia Research Group
Coordinator of this site? Confirm its status
JonesboroUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.