Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
26 participants
OBSERVATIONAL
2017-01-31
2020-02-25
Brief Summary
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Detailed Description
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Conditions
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Study Design
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COHORT
PROSPECTIVE
Study Groups
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historic control group
Work-up and follow-up of the historic control will be performed through similar means by contacting primary care physicians and/or medical oncologists, if information cannot be received, the patient will be directly contacted. In case the patient cannot be reached and no other information can be received on patients outcome, the death registry will be contacted.
No interventions assigned to this group
comparator group
All patients with potentially and borderline resectable pancreatic cancer are potentially candidates for IRE and will be considered for this treatment. Patient will be recruited/referred through daily clinical practice from the Inselspital Bern. Final inclusion into the study will be performed by the responsible investigators at the Inselspital Bern. Patients will be included according to the inclusion/exclusion criteria mentioned.
Irreversible electroporation
Interventions
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Irreversible electroporation
Eligibility Criteria
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Inclusion Criteria
* Age ≥ 18 years
* Able to undergo general anesthesia (ASA ≤ 3)
* Performance status ECOG \<=2 (Eastern Cooperative Oncology Group)
* Life expectancy of at least 6 months
* Resectable or borderline resectable proven pancreatic adenocarcinoma of the pancreas
Exclusion Criteria
* History of epilepsy
* Recent history of myocardial infarction (2 months)
* Evidence of distant metastasis (e.g. liver, lung, peritoneum)
* Informed consent cannot be given by the patient
* Known hypersensitivity to the IRE electrodes (stainless steel 304L)
* Women of childbearing potential who are pregnant, breast feeding, or not taking an adequate method of contraception at the time of procedure
18 Years
ALL
No
Sponsors
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Insel Gruppe AG, University Hospital Bern
OTHER
Responsible Party
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Principal Investigators
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Mathias Worni, MD
Role: PRINCIPAL_INVESTIGATOR
Inselspital Berne
Locations
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Inselhospital
Bern, , Switzerland
Countries
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Other Identifiers
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IRE Marg
Identifier Type: -
Identifier Source: org_study_id
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