Observational Study of Pancreatic Cysts
This observational study aims to better understand pancreatic cysts, which are often found incidentally during imaging tests. Researchers want to learn how these cysts change over time and develop better ways to tell if a cyst is harmless or has the potential to become cancerous. They will do this by looking at your medical records, including clinical information, imaging results, and biomarker (biological markers) characteristics. The goal is to improve how doctors diagnose and manage pancreatic cysts, potentially reducing unnecessary procedures for benign (non-cancerous) cysts and ensuring appropriate follow-up for those that might be more serious. You may be eligible to participate if you are an adult aged 18 or older and have been referred for a pancreatic cyst assessment. The study plans to enroll 5000 participants, but its current status is unclear.
- Study design
- This is an observational study, meaning researchers will collect information about your pancreatic cysts over time. It aims to enroll 5000 participants.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- The study will assess the clinical utility of Compcyst in pancreatic cysts as assessed by patient chart review, measured at 15 years.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Diagnostic Strategies, Risk Assessment and Progression of Pancreatic Cysts
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Elham Afghani, MD MPH · PRINCIPAL_INVESTIGATOR · Johns Hopkins University
Who to contact
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Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Clinical utility of Compcyst in pancreatic cysts as assessed by patient chart review15 years
Compcyst is part of the new standard of care diagnosis of precancerous and benign cystic lesions. Patient charts will be reviewed for clinical, radiological, surgical and pathologic information (all combined into a composite) that will be used to determine if Compcyst as part of the new standard of care is better than the diagnostic measure in the old standard of care in detecting precancerous and benign cystic lesions. Patient records over a 15-year period will be reviewed.