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Spots Global Cancer Trial Database for A Registry Study of NanoKnife IRE for Stage 3 Pancreatic Cancer

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We do not endorse or review these studies in any way.

Trial Identification

Brief Title: A Registry Study of NanoKnife IRE for Stage 3 Pancreatic Cancer

Official Title: Registry to Evaluate Effectiveness and Safety of the NanoKnife System for the Ablation of Stage 3 Pancreatic Adenocarcinoma

Study ID: NCT03899649

Interventions

SOC
NanoKnife System

Study Description

Brief 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 \[SOC cohort\].

Detailed Description:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Moores Cancer Center, UC San Diego Health, La Jolla, California, United States

University of Florida Health, Gainesville, Florida, United States

Miami Cancer Institute, Miami, Florida, United States

Wellstar Medical Group, Marietta, Georgia, United States

Northwest Community Hospital, Arlington Heights, Illinois, United States

University of Iowa Healthcare, Iowa City, Iowa, United States

Norton Healthcare, Louisville, Kentucky, United States

Mayo Clinic, Rochester, Rochester, Minnesota, United States

Barnes-Jewish Hospital, Saint Louis, Missouri, United States

NYU Langone, New York, New York, United States

Presbyterian Hospital, Columbia, New York, New York, United States

Atrium Health, Charlotte, North Carolina, United States

St. Luke's University Health Network, Easton, Pennsylvania, United States

University of Texas-Southwestern, Dallas, Texas, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

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