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Clinical Trial Summary

This is an exploratory, single center, open label, parallel-dose, and prospective study of BR55 CEUS for characterization of solid pancreatic lesions in subjects with suspected PDAC using transabdominal US.


Clinical Trial Description

Approximately twenty-four (24) subjects with suspected PDAC and scheduled to undergo surgical resection within 30 days (but not before 24 hours) after the transabdominal BR55 CEUS examination will be enrolled into 3 dose groups, 0.03, 0.05, and 0.08 mL/kg, with a maximum of 8 patients in each dose group. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03486327
Study type Interventional
Source Bracco Diagnostics, Inc
Contact
Status Active, not recruiting
Phase Phase 2
Start date July 19, 2018
Completion date March 31, 2024

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