The LINFU® U.S. Registry in Patients With Clinical Signs and/or Symptoms of Disease

Trial Title: The LINFU® U.S. Registry in Patients With Clinical Signs and/or Symptoms of Disease

NCT ID: NCT06276738

Condition: Pancreatic Cancer
Jaundice
Abdominal Neoplasm

Conditions: Official terms:
Abdominal Neoplasms
Jaundice
Pancrelipase

Study type: Observational [Patient Registry]

Overall status: Not yet recruiting

Study design:

Time perspective: Prospective

Intervention:

Intervention type: Diagnostic Test
Intervention name: LINFU® (Low Intensity Non-Focused Ultrasound excitation of the pancreas)
Description: Patients will undergo low intensity non-focused ultrasound excitation of the pancreas for a total of 15 minutes. A contrast agent will be administered IV at five minute intervals. The patient will then receive a dose of secretin and the the patient's pancreatic juice will then be collected for a total of 15 minutes.
Arm group label: Patients at increased risk for developing pancreatic cancer

Summary: Evaluate LINFU® in patients who exhibit signs or symptoms (i.e. jaundice, abdominal pain, weight loss, nausea and vomiting etc.) suggestive of pancreatic cancer (PDAC) or have evidence of imaging studies suggestive of PDAC.

Detailed description: Adenocyte has developed a proprietary pancreatic cancer detection method, LINFU®, (Low Intensity Non-Focused Ultrasound excitation of the pancreas) that increases the sensitivity of pancreatic juice cytology. LINFU® excitation of circulating microbubbles increases the exfoliation of pancreatic ductal cells. The sensitivity of cytological examination of the pancreatic fluid obtained by LINFU® can also be potentially enhanced by neural network-based computer-assisted analysis. In this study, LINFU® will be evaluated in patients who exhibit symptoms suggestive of PDAC (i.e. jaundice, abdominal pain, weight loss, nausea and vomiting etc.) or have evidence of imaging studies suggestive of PDAC. In addition, patients with PDAC identified only with LINFU® and not detected with other diagnostic tests will be followed long term to determine the progression rate of these tumors and to determine whether LINFU® results in earlier intervention, treatment and improvement in patient outcomes.

Criteria for eligibility:

Study pop:
High risk patients with either clinical symptoms or imaging abnormalities or both, being evaluated for PDAC.

Sampling method: Non-Probability Sample
Criteria:
Inclusion Criteria: - Both males and females will be enrolled and must be at least 18 years of age and under age of 90 - Patients, who in the opinion of the Investigator, require biopsy to rule out PDAC because they display at least one of the following or both: a) clinical symptoms of PDAC including jaundice, nausea and vomiting, weight loss, abdominal pain, bloating or the feeling of fullness, itchy skin, lower back pain, light-colored, greasy stools, sudden onset type 2 diabetes, etc. b) one or more imaging studies suggestive of PDAC - All patients must undergo contemporaneous imaging, either within 90 days before the LINFU® procedure or within 30 days after the procedure, with one or more of the following: EUS± FNA, MRI/MRCP, ERCP, CT or CEUS. - Institutional Review Board (IRB)-approved consent must be signed by patients to participate in this study. Exclusion Criteria: - Patient under the age of 18 and over the age 90 - Contraindications to LINFU®/EUS/ERCP as determined by study investigators: Patient with uncorrectable coagulopathy; Patient that cannot undergo anesthesia due to cardiopulmonary contraindication as deemed by the anesthesiologist; Unstable medically (cardiopulmonary, neurologic, or cardiovascular status) - Patients undergoing EUS or ERCP for a suspected bile duct cancer arising from the intrahepatic or extrahepatic biliary epithelium - Patients who are already known to have PDAC by cytologic or histologic evidence - Patients with intraductal papillary mucinous neoplasm of the pancreas (IPMN) identified either before the study or during the study through imaging evaluation will be excluded - Pregnant females will be excluded - Patient that is unable to provide informed consent - Patient with known allergy to the microbubble contrast agent or secretin

Gender: All

Minimum age: 18 Years

Maximum age: 90 Years

Healthy volunteers: Accepts Healthy Volunteers

Start date: June 30, 2024

Completion date: May 1, 2034

Lead sponsor:
Agency: Adenocyte, LLC
Agency class: Industry

Source: Adenocyte, LLC

Record processing date: ClinicalTrials.gov processed this data on November 12, 2024

Source: ClinicalTrials.gov page: https://clinicaltrials.gov/ct2/show/NCT06276738