Artificial Intelligence (AI) Cytopathology Trial

Recruiting Observational Study
Pancreatic Solid Lesions
No Placebo Group Every participant receives an active treatment — no one gets a placebo. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 100
Sex
Any
Study type
Observational
Participants needed
50 (estimated)
Sponsor
The University of Texas Health Science Center, Houston · Other
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About This Trial
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 be…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Have EUS finding of a PSL; * Do not have contraindications for FNA/FNB. Exclusion Criteria: * Inability to provide informed consent for the procedure; * Contraindication for FNA/FNB eg coagulopathy, lack of avascular window for FNA.
Contacts

Prithvi B Patil, MS

7135006456

prithvi.b.patil@uth.tmc.edu

CONTACT