RECRUITING

Pancreatic Cancer & Surgical Resection

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

AHPBA Registry Database (Collection of Clinical Data Related to Pancreatic Cancer & Treatment - Irreversible Electroporation (IRE))

Quick Facts

Study Start:2017-12-20
Study Completion:2024-12
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT05170802

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. 1. more than 18 years of age
  2. 2. Diagnosed with pancreatic cancer and has consented to undergo the NanoKnife procedure per the treating physician
  3. 3. Willing and able to comply with the protocol requirements
  4. 4. Able to comprehend and sign the Informed Consent Form in English or Spanish
  1. * Patients who meet any of the following criteria will be excluded from the study:
  2. 1. Do not meet the Study Inclusion Criteria laid out above

Contacts and Locations

Study Contact

Crystee Cooper, DHEd
CONTACT
214-947-1280
clinicalresearch@mhd.com
Zaid Haddadin, MS
CONTACT
214-947-4459
clinicalresearch@mhd.com

Principal Investigator

Alejandro Mejia, M.D.
PRINCIPAL_INVESTIGATOR
Methodist Dallas Medical Center

Study Locations (Sites)

Liver Institute of Methodist Dallas Medical Center
Dallas, Texas, 75203
United States

Collaborators and Investigators

Sponsor: Methodist Health System

  • Alejandro Mejia, M.D., PRINCIPAL_INVESTIGATOR, Methodist Dallas Medical Center

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2017-12-20
Study Completion Date2024-12

Study Record Updates

Study Start Date2017-12-20
Study Completion Date2024-12

Terms related to this study

Additional Relevant MeSH Terms

  • Pancreas Cancer