Clinical Trial Record

Return to Clinical Trials

Collection of Circulating Biomarkers in Pancreatic Cancer


2023-02-27


2027-06-30


2028-01-15


30

Study Overview

Collection of Circulating Biomarkers in Pancreatic Cancer

This protocol will involve collection of blood samples from patients with a diagnosis of pancreatic adenocarcinoma for evaluation of circulating biomarkers.

N/A

  • Pancreas Cancer
  • OTHER: Obtaining blood for analysis of various circulating biomarkers
  • UPCC 20222
  • 852628 (OTHER Identifier) (OTHER: University of Pennsylvania IRB)

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 Results Reporting Dates Study Record Updates

2023-02-10  

N/A  

2025-03-06  

2023-02-22  

N/A  

2025-03-10  

2023-02-24  

N/A  

2025-03  

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

Primary Purpose:
N/A


Allocation:
N/A


Interventional Model:
N/A


Masking:
N/A


Arms and Interventions

Participant Group/ArmIntervention/Treatment
: Blood specimens

Collection of blood for analysis of various circulating biomarkers in patients with pancreatic adenocarcinoma.

OTHER: Obtaining blood for analysis of various circulating biomarkers

  • 4 tbsp of blood in a 1-week period, occurring no more frequently than 4 times in an 8-week period
Primary Outcome MeasuresMeasure DescriptionTime Frame
To create a comprehensive system to collect, catalogue and store blood specimens from subjects with pancreatic cancer for future research use.Through study completion, an average of 1 year
Secondary Outcome MeasuresMeasure DescriptionTime Frame
To create a computerized clinical data set from subjects with pancreatic cancer that contains information related to the subject's general health, disease status, treatments, and response.Through study completion, an average of 1 year
To integrate the data and specimens to permit the most informative clinical-biologic research platform.Through study completion, an average of 1 year

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Study Contact

Name: Liudmila Mazaleuskaya, PhD

Phone Number: 267-455-9141

Email: mazali@pennmedicine.upenn.edu

Study Contact Backup

Name: Mark O'Hara, MD

Phone Number: 215-360-0919

Email: Mark.OHara@pennmedicine.upenn.edu

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:
ALL

Sexes Eligible for Study:
18 Years

Accepts Healthy Volunteers:

    Inclusion Criteria:

  • The subject must have a known or presumed diagnosis of pancreatic adenocarcinoma
  • The subject must be a patient of the University of Pennsylvania
  • The subject must be able to provide informed consent
  • The subject must be 18 years of age or older

  • Exclusion Criteria:
    . Subjects who have any clinically significant psychiatric, social, or medical condition that, in the opinion of the investigator, could increase the patient's risk, interfere with protocol adherence, or affect the patient's ability to give informed consent are ineligible to participate in the study.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.


    • PRINCIPAL_INVESTIGATOR: Mark O'Hara, MD, Abramson Cancer Center, University of Pennsylvania

    Publications

    The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

    General Publications

    No publications available