[{"data":1,"prerenderedAt":-1},["ShallowReactive",2],{"health-studies-list:{\"overallStatus\":[\"RECRUITING\",\"AVAILABLE\",\"NOT_YET_RECRUITING\"],\"leadSponsorName\":\"Adenocyte, LLC\",\"orderBy\":\"LastUpdateSubmitDate:desc\",\"size\":25,\"offset\":0}":3,"health-study-condition:":63},{"pageToken":4,"total":5,"offset":6,"count":5,"results":7},null,2,0,[8,42],{"id":9,"slug":10,"hasResults":11,"nctId":12,"briefTitle":13,"officialTitle":14,"acronym":4,"eligibilityCriteria":15,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":20,"targetDuration":23,"studyType":24,"phases":4,"briefSummary":25,"conditions":26,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":31,"lastUpdatePostDateStruct":32,"startDateStruct":35,"completionDateStruct":37,"leadSponsor":39,"locationsCount":4},"100537359","the-linfu-us-registry-for-the-in-the-general-population-without-risk-factors-100537359",false,"NCT06276803","The LINFU® U.S. Registry for the in the General Population Without Risk Factors","The LINFU® U.S. Registry for the Detection of Low and High-Grade Atypia and Early, Asymptomatic Pancreatic Ductal Adenocarcinoma (PDAC) in the General Population Without Risk Factors","Inclusion Criteria:\n\n1. Both males and females will be enrolled and must be at least 18 years of age and under age of 90\n2. Patients, who in the opinion of the Investigator, do not exhibit any 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.\n3. Patients, who in the opinion of the Investigator, do not have an abnormal imaging study suggestive of PDAC\n4. Patients, who in the opinion of the Investigator, should not be ordinarily screened for PDAC because they do not have risk factors including chronic pancreatitis, family history of PDAC, or genetic cancer syndromes which increase the risk of developing PDAC\n5. Institutional Review Board (IRB)-approved consent must be signed by patients to participate in this study.\n\nExclusion Criteria:\n\n1. Patient under the age of 18 and over the age 90\n2. Contraindications to LINFU®\u002FEUS\u002FERCP as determined by study investigators:\n\n   1. Patient with uncorrectable coagulopathy\n   2. Patient that cannot undergo anesthesia due to cardiopulmonary contraindication as deemed by the anesthesiologist\n   3. Unstable medically (cardiopulmonary, neurologic, or cardiovascular status)\n3. Patients, who in the opinion of the Investigator, are at risk of PDAC because they exhibit any of the following: clinical symptoms of PDAC, imaging abnormalities suggestive of PDAC, genetic syndromes which increase the risk of PDAC, a first degree relative with a history of pancreatic cancer, excessive exposure to dry-cleaning and metalworking chemicals\n4. Patients who consume alcohol (greater than 3 drinks\u002Fday \\>1 year or \\>15g\u002Fday for \\>1 year will be excluded\n5. Patient with any history of adult-onset diabetes will be excluded\n6. Patients who are obese (body mass index \\[BMI\\] of 30 or more) will be excluded\n7. Patients who have consumed tobacco in the past for greater than 1 year or current smokers will be excluded.\n8. Patients with a history of any pancreatic disease, including chronic pancreatitis, or any pancreatic imaging abnormality including intraductal papillary mucinous neoplasm of the pancreas (IPMN)\n9. Patients with baseline lipase levels that are abnormal\n10. Pregnant females will be excluded\n11. Patient that is unable to provide informed consent\n12. Patient with known allergy to the microbubble contrast agent or secretin",true,"ALL","18 Years","90 Years",{"count":21,"type":22},500,"ESTIMATED","5 Years","OBSERVATIONAL","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.. In this study, LINFU® will be evaluated in the general population with no risk factors and who exhibit no signs or symptoms of disease, This study will help determine if LINFU® can be used to help identify early, asymptomatic pancreatic ductal adenocarcinoma (PDAC) or their precursor lesions (PanIn-2, PanIn-3).",[27,28,29],"Pancreatic Cancer","Pancreatic Ductal Adenocarcinoma","Pancreatic Dysplasia","NOT_YET_RECRUITING","2024-07-30",{"date":33,"type":34},"2024-07-31","ACTUAL",{"date":36,"type":22},"2024-09-15",{"date":38,"type":22},"2034-12-15",{"name":40,"class":41},"Adenocyte, LLC","INDUSTRY",{"id":43,"slug":44,"hasResults":11,"nctId":45,"briefTitle":46,"officialTitle":47,"acronym":4,"eligibilityCriteria":48,"healthyVolunteers":16,"sex":17,"minAge":18,"maxAge":19,"enrollmentInfo":49,"targetDuration":23,"studyType":24,"phases":4,"briefSummary":51,"conditions":52,"keywords":4,"overallStatus":30,"whyStopped":4,"lastUpdateSubmitDate":55,"lastUpdatePostDateStruct":56,"startDateStruct":58,"completionDateStruct":60,"leadSponsor":62,"locationsCount":4},"100537354","the-linfu-us-registry-in-patients-with-clinical-signs-andor-symptoms-of-disease-100537354","NCT06276738","The LINFU® U.S. Registry in Patients With Clinical Signs and\u002For Symptoms of Disease","The LINFU® U.S. Registry for the Detection of Pancreatic Ductal Adenocarcinoma (PDAC) in Patients With Clinical Signs and\u002For Symptoms of Disease","Inclusion Criteria:\n\n* Both males and females will be enrolled and must be at least 18 years of age and under age of 90\n* 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\n* 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\u002FMRCP, ERCP, CT or CEUS.\n* Institutional Review Board (IRB)-approved consent must be signed by patients to participate in this study.\n\nExclusion Criteria:\n\n* Patient under the age of 18 and over the age 90\n* Contraindications to LINFU®\u002FEUS\u002FERCP 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)\n* Patients undergoing EUS or ERCP for a suspected bile duct cancer arising from the intrahepatic or extrahepatic biliary epithelium\n* Patients who are already known to have PDAC by cytologic or histologic evidence\n* 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\n* Pregnant females will be excluded\n* Patient that is unable to provide informed consent\n* Patient with known allergy to the microbubble contrast agent or secretin",{"count":50,"type":22},1000,"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.",[27,53,54],"Jaundice","Abdominal Neoplasm","2024-05-12",{"date":57,"type":34},"2024-05-14",{"date":59,"type":22},"2024-06-30",{"date":61,"type":22},"2034-05-01",{"name":40,"class":41},""]