Clinical Trials

Clinical Trials

Clinical Trial Number: PROPEL
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Galvanize Prospective/​Retrospective Pulsed Electric Field Device Registry

Study ID: PROPEL
Phase N/A
Physician Investigator(s)
Study Locations

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484.476.2649
cancertrials@mlhs.org

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.

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Eligibility Criteria

Inclusion Criteria:

  1. Subject will undergo or has undergone PEF energy delivery utilizing Galvanize technology
  2. Subject is expected to be available for follow-up per the enrolling physician's standard care practices
  3. For prospective cohort, subject has a life expectancy of at least 3 months; for retrospective cohort, subject has completed at least three months of imaging following the PEF procedure
  4. Signed informed consent is obtained, if required by IRB

Exclusion Criteria:

None