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NCT Number: NCT07651852

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

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).

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Key Inclusion Criteria:

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

Key Exclusion Criteria:

  • Patients whose life expectancy is 1 year or less
  • Contraindication to left atrial catheter ablation or PF ablation
  • Current enrollment in any investigational study of a medical device, biologic, or drug not pre-approved by Kardium

Treatment and study plan

Globe Pulsed Field System

Device

Ablation and atrial mapping with the Globe Pulsed Field System

Primary outcomes

  1. Effectiveness endpoint

    Time frame: 12 months

    Rate of 12-month treatment success following ablation using the Globe PF System.

  2. Safety endpoint

    Time frame: 7 days

    Rate of subjects with one or more major adverse events up to 7 days following the index ablation procedure.

Study contacts

Contact information is provided by the study sponsor or research team.

Clinical Affairs

CONTACT

[email protected]

+1 (604) 248 8891

Sponsors and collaborators

Lead sponsor

Kardium Inc.

Industry

Registry information

Important dates

Study start
2026
Primary completion
2029
Study completion
2029
First posted
Jun 16, 2026
Registry last updated
Jun 16, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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