Pancreatic Cancer & Surgical Resection

Status unconfirmed

Conditions studied: Pancreas Cancer

In brief

Primary Objective(s) To collect clinical data related to the treatment outcomes of Pancreatic IRE in order to develop an evidence base such that physicians can provide the best possible care to patients with pancreatic cancer requiring surgical intervention. Secondary Objective(s) To collect data on adverse events and complications related to IRE treatment. The AHPBA (Americas Hepato-Pancreato-Biliary Association) will be responsible for data collection and will periodically audit the data for quality assurance purposes. The AHPBA will review outcomes reported by each participating Research Institution and if outcomes are in the lower percentile, the investigators will be offered support to analyze the reasons for the suboptimal outcomes and may seek support to improve outcomes. The participating Research Institutions will receive a certificate annually that acknowledges their participation in the Research Project.

Key facts

Study ID

NCT05170802

Run by

Methodist Health System

People needed

30

Starts

2017-12-20

Expected to finish

2024-12-01

Last updated by the study team

2024-03-27

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• more than 18 years of age
• Diagnosed with pancreatic cancer and has consented to undergo the NanoKnife procedure per the treating physician
• Willing and able to comply with the protocol requirements
• Able to comprehend and sign the Informed Consent Form in English or Spanish

You may not qualify if…

• Patients who meet any of the following criteria will be excluded from the study:
• Do not meet the Study Inclusion Criteria laid out above

Where it is running

• Liver Institute of Methodist Dallas Medical Center — Dallas, Texas, United States (enrolling)

Full record on ClinicalTrials.gov

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