Registry of Pancreatic Disease
PAD-R
Registry of Subjects Affected by Pancreatic Disease and Evaluated at the Pancreas Institute of Verona
1 other identifier
observational
3,000
1 country
1
Brief 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.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P75+ for all trials
Started Dec 2016
Longer than P75 for all trials
1 active site
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
Click on a node to explore related trials.
Study Timeline
Key milestones and dates
Study Start
First participant enrolled
December 1, 2016
CompletedFirst Submitted
Initial submission to the registry
January 15, 2019
CompletedFirst Posted
Study publicly available on registry
January 17, 2019
CompletedPrimary Completion
Last participant's last visit for primary outcome
December 1, 2046
ExpectedStudy Completion
Last participant's last visit for all outcomes
December 1, 2046
January 17, 2019
January 1, 2019
30 years
January 15, 2019
January 15, 2019
Conditions
Outcome Measures
Primary Outcomes (1)
Overall survival
Survival from Diagnosis to time of death
1 year
Secondary Outcomes (1)
Postoperative morbidity
90 days
Study Arms (1)
Patient with pancreatic disease
Patients diagnosed with pancreatic disease evaluated at this institution.
Eligibility Criteria
Every patient affected by pancreatic disease admitted to General and Pancreatic Surgery Department of Verona University Hospital from 01/01/1990 to 12/01/2046
You may qualify if:
- any type of pancreatic disease: inflammatory and neoplastic (including solid and cystic lesions)
You may not qualify if:
- physically or mentally inability to provide consent
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
AOUI Verona
Verona, 37124, Italy
MeSH Terms
Conditions
Condition Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Claudio Bassi, Prof
AOUI Verona
Central Study Contacts
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- OTHER
- Target Duration
- 27 Years
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
January 15, 2019
First Posted
January 17, 2019
Study Start
December 1, 2016
Primary Completion (Estimated)
December 1, 2046
Study Completion (Estimated)
December 1, 2046
Last Updated
January 17, 2019
Record last verified: 2019-01