Protocol to Permit the Acquisition of Circulating Tumor Material in Pancreatic Diseases
1 other identifier
observational
100
1 country
1
Brief Summary
The purpose of this study is to collect blood samples to detect potential markers of pancreatic cancer in the blood and link these findings to medical and health information. Information from this study may help to provide insight into the detection of pancreas cancer in the blood before it can be found by other methods or provide a method of monitoring the status of pancreatic cancer throughout a treatment course. Another purpose of this study is to collect blood to create a biobank.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P50-P75 for all trials
Started Sep 2015
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
June 11, 2015
CompletedFirst Posted
Study publicly available on registry
June 15, 2015
CompletedStudy Start
First participant enrolled
September 10, 2015
CompletedPrimary Completion
Last participant's last visit for primary outcome
January 1, 2035
ExpectedStudy Completion
Last participant's last visit for all outcomes
January 1, 2035
April 4, 2025
April 1, 2025
19.3 years
June 11, 2015
April 3, 2025
Conditions
Outcome Measures
Primary Outcomes (1)
Collection of blood and tissue samples from subjects with pancreatic diseases
3 years
Eligibility Criteria
subjects with pancreatic diseases
You may qualify if:
- The subject must be a patient at the Hospital of the University of Pennsylvania
- The subject must be under evaluation and/or treatment for a pancreatic disease
- The subject must be under evaluation and/or treatment for a non-pancreatic disease. For example, patients undergoing routine colonoscopy within the clinical practice will be asked to consent to provide control samples.
- The subject must be able to provide informed consent or have an acceptable surrogate capable of giving consent on the subject's behalf
- The subject must be 18 years of age or older
You may not qualify if:
- The subject or acceptable surrogate does not provide informed consent
- Subject is a prisoner
- Subject is under 18 years of age
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Abramson Cancer Center of the University of Pennsylvania
Philadelphia, Pennsylvania, 19104, United States
Biospecimen
The frequency of research blood collection will not exceed 60 mL in a 1 week period and will not occur more frequently than 4 times in an 8 week period.
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Peter O'Dwyer, MD
Abramson Cancer Center at Penn Medicine
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- PROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
June 11, 2015
First Posted
June 15, 2015
Study Start
September 10, 2015
Primary Completion (Estimated)
January 1, 2035
Study Completion (Estimated)
January 1, 2035
Last Updated
April 4, 2025
Record last verified: 2025-04