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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT03140592
Other study ID # IRBNet # 618834
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date January 14, 2015
Est. completion date January 2023

Study information

Verified date March 2021
Source Stony Brook University
Contact Jonathan Buscaglia, MD
Phone 6314447225
Email jonathan.buscaglia@stonybrookmedicine.edu
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Pancreatic cancer is a very aggressive cancer. Over the past 40 years there has not been much progress made in reducing deaths from this cancer. Recently, new models of pancreatic cancers have been generated from mouse and human tissues. These models have used larger pieces of tissues taken from surgical removal of pancreatic cancers. The purpose of this study is to determine whether these new pancreatic cancer models can be generated from the small biopsies we take to make the diagnosis of the pancreatic mass.


Description:

The Endoscopic Ultrasound guided pancreatic biopsy tissue collected for only research purposes will be used to generate organoids in a in-vivo and in-vitro setting. The development of these methods may help scientists identify new treatments for pancreatic cancer and to potentially develop more personalized approaches to treating pancreatic cancer.


Recruitment information / eligibility

Status Recruiting
Enrollment 300
Est. completion date January 2023
Est. primary completion date January 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: 1. Patients who are scheduled for an EUS-FNB of pancreatic mass(es) suspicious for pancreatic ductal adenocarcinoma performed by a member of the Stony Brook Interventional Endoscopy Section of the Division of Gastroenterology and Hepatology 1. Age = 18 years 2. Literate and able/willing to provide informed consent for participation in research. Exclusion Criteria: 1. Age < 18 years 2. Not literate or unable/unwilling to provide informed consent for EUS-FNB research biopsies 3. Pregnancy as determined by serum or urine HCG test performed as standard of clinical care for all women of childbearing age and documented on subjects' electronic medical record

Study Design


Intervention

Procedure:
Biopsy
Two extra EUS guided pancreatic biopsies collected for only research purposes.

Locations

Country Name City State
United States Stony Brook University Stony Brook New York

Sponsors (1)

Lead Sponsor Collaborator
Stony Brook University

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Successful generation of pancreatic organoids The two extra biopsy tissues collected for only research purposes will be used to generate pancreatic organoids in a in-vivo as well as in-vitro setting. 6 years
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