The LINFU® U.S. Registry for the Detection of Asymptomatic Pancreatic Ductal Adenocarcinoma
Part of paid clinical trials in New York, New York.
- Sponsor
- Adenocyte, LLC
- Study ID
- NCT06157671
- Status
- Enrolling By Invitation
Conditions
- Pancreatic Adenocarcinoma
- Pancreatic Intraepithelial Neoplasia
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - 90 Years
- Healthy Volunteers
- Not accepted
Study Details
Adenocyte has developed LINFU®, (Low Intensity Non-Focused Ultrasound excitation of the pancreas) as a method of identifying early, asymptomatic pancreatic cancer and its noninvasive precancerous lesions. The test involves ultrasound and an analysis of pancreatic juice. A neural network-based computer-assisted system may be utilized to enhance the analysis. Patients enrolled are being screened for pancreatic cancer because they have known risk factors (i.e. smoking, diabetes, chronic pancreatitis, family history of pancreatic cancer, or certain genetic syndromes).
Key Dates
- Start date
- Jan 31, 2024
- Status verified
- Mar 2025
- Primary completion
- Jan 1, 2030
- Completion
- Jun 1, 2030
Study Design
- Enrollment
- 1,000 participants (estimated)
Arms
- Arm: Patients at increased risk for developing pancreatic cancerPatients being screened for pancreatic cancer because they have known risk factors (i.e. smoking, diabetes, chronic pancreatitis, family history of pancreatic cancer, or certain genetic syndromes) and are undergoing other imaging diagnostic tests to determine if they have pancreatic cancer
Primary Outcome Measure
The number of pancreatic ductal adenocarcinomas and their noninvasive precursor lesions identified only with LINFU® will be compared to standard screening methods [ Time Frame: 5 years ]
Locations (1)
| Facility | City | State | ZIP | Site coordinators |
|---|---|---|---|---|
| Manhattan Endoscopy Center | New York | New York | 10017 | - |
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