Actively Recruiting
A Study for the PanCystPro Assay in the Management of Pancreatic Cystic Lesions
Led by Amplified Sciences Inc · Updated on 2026-03-16
50
Participants Needed
3
Research Sites
71 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The purpose of this research is to learn if the PanCystPro assay can help doctors in making decisions about treatment and monitoring of pancreatic cysts. The PanCystPro test measures glucose, carcinoembryonic antigen (CEA), and gastricsin biomarkers on fluid obtained from a pancreatic cyst. The test reports if the cyst fluid should be considered "Non-mucinous" or "Mucinous". Mucinous pancreatic cysts are more likely to progress to cancer while non-mucinous cysts seldom progress to cancer.
CONDITIONS
Official Title
A Study for the PanCystPro Assay in the Management of Pancreatic Cystic Lesions
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients 18 years of age or older
- Pancreatic cyst at least 12 mm in size confirmed by imaging where fluid sampling can help manage care
- Signed written informed consent
- Undergoing Endoscopic Ultra Sound (EUS) with planned Fine Needle Aspirate (FNA) as part of standard care
You will not qualify if you...
- Diagnosis of pancreatic cancer
- Pregnant or lactating females
- Contraindications to moderate or deep sedation required for endoscopic ultrasound, such as major heart or lung illness
- Contraindications to Fine Needle Aspirate of pancreatic cyst, including use of blood thinners
AI-Screening
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Trial Site Locations
Total: 3 locations
1
Indiana University
Indianapolis, Indiana, United States, 46202
Actively Recruiting
2
Beth Israel Deaconess Medical Center
Boston, Massachusetts, United States, 02215
Actively Recruiting
3
Rutgers Health
New Brunswick, New Jersey, United States, 08901
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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