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Clinical Trial Summary

This is a randomized study that will enroll patients scheduled for an endoscopic ultrasound biopsy of a pancreas lesion to be in the heparin or saline group during the procedure. The purpose of this study is to examine the effect of blood contamination, heparin priming of the fine needle biopsies, and pass number on tumor tissue quality in fine needle biopsies. The hypothesis for this study is that fine needle biopsy tissue quality of pancreatic masses decreases with increasing pass number due to blood contamination; this blood contamination can be ameliorated with priming of the needle with an anticoagulant such as heparin.


Clinical Trial Description

This study was amended at the Institutional Review Board (IRB) after having enrolled only two participants. Following the amendment, the responsible party changed and with that change some adjustments were made to the interventions, analysis and some outcomes. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT04764396
Study type Interventional
Source University of Michigan
Contact Eileen Carpenter, MD
Phone 734-936-4385
Email eicarpen@umich.edu
Status Recruiting
Phase N/A
Start date March 12, 2021
Completion date August 2025

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