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Galvanize Prospective/Retrospective Pulsed Electric Field Device Registry

NCT05851430 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 1000

Last updated 2026-04-23

No results posted yet for this study

Summary

The goal of this observational registry is to assess the use and performance of Galvanize PEF technology in a real-world setting. The main questions it aims to answer are:

* PEF utilization and performance
* Monitor safety outcomes and inform future generation devices.

Participants will undergo the PEF procedure and be followed per institutional standard of care.

Conditions

  • Soft Tissue Lesion

Interventions

DEVICE

PEF ablation

Pulsed Electric Field (PEF) Ablation per institutional standard of care

Sponsors & Collaborators

  • Galvanize Therapeutics, Inc.

    lead INDUSTRY

Principal Investigators

  • William Krimsky, MD · Chief Medical Officer

Eligibility

Min Age
18 Years
Max Age
100 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-06-23
Primary Completion
2028-06-30
Completion
2028-12-31
FDA Device
Yes

Countries

  • United States

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT05851430 on ClinicalTrials.gov