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Behandeling met het Nanoknife® systeem bij patiënten met alvleesklierkanker die niet operatief verwijderd kan worden.

Recruiting
Conditions
pancreatic cancer, pancreatic adenocarcinoma, local ablative therapy, irreversible electroporationalvleesklierkanker, pancreascarcinoom, lokale ablatietherapie, irreversibele electroporatie
Registration Number
NL-OMON20237
Lead Sponsor
AMC Amsterdam
Brief Summary

/A

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Not specified
Target Recruitment
106
Inclusion Criteria

•Age 18 years or older

•Capable of providing written and oral informed consent

Exclusion Criteria

•Resectable pancreatic cancer during explorative laparotomy

•Presence of metastatic disease (peritoneal, liver or other)

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The primary outcome is the effect of IRE on severe morbidity and mortality occurring until 90 days after IRE treatment. Severe morbidity is defined as defined as Clavien-Dindo score 3 or more.
Secondary Outcome Measures
NameTimeMethod
Secondary outcomes are the success rate of completing IRE procedure, duration of IRE procedure, intraprocedural complications, the impact of IRE on functional recovery, hospital stay, adverse events, need for re-interventions and readmissions and, effects on survival rates (2-year survival, median survival, progression free survival). <br>Other study parameters are baseline characteristics
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