A Registry Study of NanoKnife IRE for Stage 3 Pancreatic Cancer
Condition(s) studied
Investigational drug(s) / intervention(s)
SOC: Standard of Care treatment
NanoKnife System: Irreversible Electroporation
Study summary
This multicenter, observational study will evaluate the effectiveness and safety of the NanoKnife System when used for the ablation of Stage 3 pancreatic adenocarcinoma (Stage 3 PC). Eligible patients will be recruited over a 36-month period and participating institutions will enroll and provide data on consecutive patients that meet inclusion and exclusion criteria. Each patient will be followed up for the duration of the study or until death. The study will include two (2) cohorts: patients who received standard of care (SOC) and received irreversible electroporation (IRE) \[IRE cohort\], and patients who were treated with SOC and did not receive IRE \[SOC cohort\].
Eligibility
Primary outcome measure(s)
- Overall Survival — Time (in months) from time of enrollment to the date of death for any reason, assessed up to 24 months.
To evaluate the effectiveness of the NanoKnife System when used for the ablation of Stage 3 PC in real world treatment settings, by testing the hypothesis that IRE with the NanoKnife System improves overall survival (OS)
Trial sites (14)
| Facility | City | Region | Status |
|---|---|---|---|
| Moores Cancer Center, UC San Diego Health | La Jolla | California | |
| University of Florida Health | Gainesville | Florida | |
| Miami Cancer Institute | Miami | Florida | |
| Wellstar Medical Group | Marietta | Georgia | |
| Northwest Community Hospital | Arlington Heights | Illinois | |
| University of Iowa Healthcare | Iowa City | Iowa | |
| Norton Healthcare | Louisville | Kentucky | |
| Mayo Clinic, Rochester | Rochester | Minnesota | |
| Barnes-Jewish Hospital | St Louis | Missouri | |
| NYU Langone | New York | New York | |
| Presbyterian Hospital, Columbia | New York | New York | |
| Atrium Health | Charlotte | North Carolina | |
| St. Luke's University Health Network | Easton | Pennsylvania | |
| University of Texas-Southwestern | Dallas | Texas |
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This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
View NCT03899649 on ClinicalTrials.gov ↗ ← All trials in the USA