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Clinical Trials/NCT02471170
NCT02471170
Enrolling By Invitation
Not Applicable

Protocol to Permit the Acquisition of Circulating Tumor Material in Pancreatic Diseases

Abramson Cancer Center at Penn Medicine1 site in 1 country100 target enrollmentSeptember 10, 2015

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pancreatic Diseases
Sponsor
Abramson Cancer Center at Penn Medicine
Enrollment
100
Locations
1
Primary Endpoint
Collection of blood and tissue samples from subjects with pancreatic diseases
Status
Enrolling By Invitation
Last Updated
last year

Overview

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.

Registry
clinicaltrials.gov
Start Date
September 10, 2015
End Date
January 1, 2035
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • 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

Exclusion Criteria

  • The subject or acceptable surrogate does not provide informed consent
  • Subject is a prisoner
  • Subject is under 18 years of age

Outcomes

Primary Outcomes

Collection of blood and tissue samples from subjects with pancreatic diseases

Time Frame: 3 years

Study Sites (1)

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