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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05743049
Other study ID # UPCC 20222
Secondary ID 852628
Status Recruiting
Phase
First received
Last updated
Start date February 27, 2023
Est. completion date February 15, 2024

Study information

Verified date October 2023
Source Abramson Cancer Center at Penn Medicine
Contact Liudmila Mazaleuskaya, PhD
Phone 267-455-9141
Email mazali@pennmedicine.upenn.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

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


Recruitment information / eligibility

Status Recruiting
Enrollment 30
Est. completion date February 15, 2024
Est. primary completion date January 30, 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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.

Study Design


Related Conditions & MeSH terms


Intervention

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

Locations

Country Name City State
United States Abramson Cancer Center at University of Pennsylvania Philadelphia Pennsylvania

Sponsors (1)

Lead Sponsor Collaborator
Abramson Cancer Center at Penn Medicine

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary 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 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
Secondary To integrate the data and specimens to permit the most informative clinical-biologic research platform. Through study completion, an average of 1 year
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