Secretin (ChiRhoStim) Pancreas Perfusion for Pancreatic Adenocarcinoma
Pancreatic Cancer

About this trial
This is an interventional diagnostic trial for Pancreatic Cancer focused on measuring Diabetes mellitus, Peutz-Jeghers syndrome
Eligibility Criteria
Inclusion Criteria:
- Persons 50 years or older with recently diagnosed diabetes (within 2 years), with at least one of the following: no family history of diabetes, abdominal discomfort, anorexia, weight loss, elevated serum CA 19-9, or those undergoing EUS with or without Fine Needle Aspiration (FNA) for pancreatic cancer screening ; OR
- Persons 35 years old or older with familial pancreatic cancer with 2 or more first degree relatives with pancreatic cancer; OR
- Persons 35 years old or older with Peutz-Jeghers syndrome; OR
- Persons 35 years old or older with suspicious clinical symptoms of pancreatic cancer, but had normal CT of the abdomen with iodinated contrast within 2 weeks.
Exclusion Criteria:
- Persons with contraindication to iodinated contrast
- Allergy to iodinated contrast
- Renal insufficiency (serum creatinine > 1.5 mg/dl)
- Patients with contraindication to ionizing radiation
- Pregnancy
- Patients with previous pancreatic surgery
- Contraindication to secretin
- Allergy to secretin
- Acute pancreatitis
Sites / Locations
- Mayo Clinic
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm 4
Experimental
Experimental
Experimental
Experimental
New Onset Diabetes
Familial Pancreatic Cancer
Peutz-Jeghers Syndrome
Clinical Symptoms of Pancreatic Cancer, Normal CT
Adults diagnosed diabetes within two years, and at least one of the following: no family history of diabetes, abdominal discomfort, anorexia, weight loss, elevated serum cancer antigen 19-9 (CA 19-9), or those undergoing endoscopic ultrasound (EUS) with or without Fine Needle Aspiration (FNA) for pancreatic cancer screening. All subjects on this arm will receive Synthetic Human Secretin as a 0.2mcg/kg one time dose prior to CT imaging on Day 1 of the study.
Adults age 35-99 with familial pancreatic cancer with two or more first degree relatives with pancreatic cancer. All subjects on this arm will receive Synthetic Human Secretin as a 0.2mcg/kg one time dose prior to CT imaging on Day 1 of the study.
Adults age 35-99 with Peutz-Jeghers syndrome. All subjects on this arm will receive Synthetic Human Secretin as a 0.2mcg/kg one time dose prior to CT imaging on Day 1 of the study.
Adults age 35-99 with suspicious clinical symptoms of pancreatic cancer, but had normal CT of the abdomen with iodinated contrast within 2 weeks. All subjects on this arm will receive Synthetic Human Secretin as a 0.2mcg/kg one time dose prior to CT imaging on Day 1 of the study.