Registry of Pancreatic Disease
NCT03807687 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 3000
Last updated 2019-01-17
Summary
This clinical data registry records information about the health status and healthcare performances received by participants affected by every type of pancreatic disease or disorder. All data (demographic, clinical, biochemical, radiological, pharmacological, genetic...) and audio and/or video recording from operative room are collected in order to be used for prospective or retrospective studies.
Conditions
- Pancreatic Diseases
- Pancreatic Neoplasms
- Pancreatitis
Sponsors & Collaborators
-
Azienda Ospedaliera Universitaria Integrata Verona
lead OTHER
Principal Investigators
-
Claudio Bassi, Prof · AOUI Verona
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2016-12-01
- Primary Completion
- 2046-12-01
- Completion
- 2046-12-01
Countries
- Italy
Study Locations
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