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Clinical Trial Summary

Purpose The primary objective of the study is to compare interpretation of EUS FNA/FNB samples for adequacy between ROSE and AI at bedside. To compare accuracy of preliminary diagnosis results between ROSE and AI at bedside versus final pathology report. Research design This is a prospective single center study to compare performance characteristics in the interpretation of EUS FNA/FNB samples between AI and ROSE. Procedures to be used Eligible patients will undergo EUS guided FNA/FNA of PSLs using standard of care. Sample slides are prepared by a cytopathologist at bedside and observed under a microscope. At the same time, the slides are scanned using a slide scanner and those images are saved for interpretation by AI at a later time.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05018663
Study type Observational
Source The University of Texas Health Science Center, Houston
Contact Prithvi B Patil, MS
Phone 7135006456
Email prithvi.b.patil@uth.tmc.edu
Status Recruiting
Phase
Start date July 21, 2021
Completion date January 30, 2028

See also
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Completed NCT03821974 - The Comparison of Wet Suction and Dry Suction Technique in EUS-FNA for the Outcomes in Pancreatic Solid Lesions N/A
Completed NCT01936467 - Comparison of Two Needle Aspiration Techniques for Endoscopic Ultrasound-guided Fine Needle Aspiration (EUS-FNA) in Solid Pancreatic Lesions Phase 3
Completed NCT04924725 - Prospective Comparison of Diagnostic Accuracy Between Contrast-enhanced Harmonic and Conventional EUS-guided Fine-needle Biopsy in Solid Pancreatic Lesions N/A