About this trial
The goal of this study is to collect biospecimens (blood and cystic fluid) and data from participants who have a pancreatic cyst that requires surgical resection. The blood and fluid samples will be analyzed for research into DNA, RNA, and proteins.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
Voluntarily agree to participate by giving written informed consent prior to any study-specific procedures.
Subject at least 18 years of age and able to provide consent. Subject is willing and able to comply with requirements of the protocol.
Radiologically documented cyst of the pancreas for which surgical removal is clinically indicated.
Patient will be undergoing a surgical resection of their pancreatic cystic neoplasm.
Disqualifiers
Patient who is pregnant at the time of study enrollment and sample collection.
Patient will not be undergoing clinically indicated surgery for a pancreatic cystic neoplasm.
Patient is unwilling or unable to provide informed consent or comply with study procedures.
Trial population
Participants will, primarily, be patients of the clinical Investigators at HOAG and Piedmont Healthcare hospitals who are or will be scheduled for surgical resection of their worrisome pancreatic cyst as part of their clinically indicated care.
Trial design
Case-only
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Characterize the miRNA and protein signatures in exosomes derived from blood and cyst fluids in patients with worrisome cystic pancreatic tumors
Sponsors and contacts
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Translational Genomics Research Institute
Lead sponsor
Hoag Memorial Hospital Presbyterian
Collaborator
City of Hope National Medical Center
Collaborator
Piedmont Healthcare
Collaborator