- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT05845801
Prospective Registry of Young-Adult Patients Diagnosed With Pancreatic Cancer (PanC-YOUNG)
May 3, 2023 updated by: Azienda Ospedaliera Universitaria Integrata Verona
The objective of the present registry is the creation of a prospective registry collecting clinico-pathological and genomic data, along with survival outcomes, of individuals diagnosed with PDAC at or before the age of 55 years old.
This registry is intended with the aim of using collected data for future clinical trials, both prospective and retrospective.
Study Overview
Status
Recruiting
Conditions
Intervention / Treatment
Study Type
Observational
Enrollment (Anticipated)
3000
Contacts and Locations
This section provides the contact details for those conducting the study, and information on where this study is being conducted.
Study Contact
- Name: Fabio Casciani
- Phone Number: 0458124671
- Email: fabio.casciani@univr.it
Study Locations
-
-
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Verona, Italy, 37134
- Recruiting
- AOUI Verona
-
Contact:
- Elisa Venturini
- Phone Number: 0458124671
- Email: elisa.venturini@univr.it
-
-
Participation Criteria
Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.
Eligibility Criteria
Ages Eligible for Study
- Adult
Accepts Healthy Volunteers
N/A
Sampling Method
Non-Probability Sample
Study Population
The target population is represented by individuals who have received a pathological diagnosis of pancreatic cancer before the age of 55 years old (namely, EO-PDAC patients).
No subject will be financially compensated for their participation.
Description
Inclusion Criteria:
- Age ≤55 years old at the time of diagnosis of pancreatic cancer
- Age ≥ 18 years
- Written informed consent obtained.
Exclusion Criteria:
- Any pancreatic neoplasm other than pancreatic cancer (e.g. cholangiocarcinoma, ampullary cancer,duodenal cancer, non-invasive mucinous cystic neoplasm, pancreatic intra-epithelial neoplasia 1 and 2, non-invasive intraductal papillary mucinous neoplasm, serous cystic neoplasm, pseudo papillary solid tumor, neuroendocrine tumor)
- Absence of informed consent.
- Age < 18 years or > 55 years old at the time of diagnosis of pancreatic cancer
Study Plan
This section provides details of the study plan, including how the study is designed and what the study is measuring.
How is the study designed?
Design Details
What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Measure Description |
Time Frame |
|---|---|---|
|
Register of young PDAC patients
Time Frame: 30 years
|
Prospective collection of epidemiological, clinical, and pathological data of patients diagnosed with early-onset pancreatic cancer (EO-PDAC) - namely, individuals who have received a diagnosis of pancreatic cancer before, or at, the age of 55 years old.
|
30 years
|
Collaborators and Investigators
This is where you will find people and organizations involved with this study.
Study record dates
These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.
Study Major Dates
Study Start (Actual)
December 7, 2022
Primary Completion (Anticipated)
September 30, 2052
Study Completion (Anticipated)
September 30, 2052
Study Registration Dates
First Submitted
April 7, 2023
First Submitted That Met QC Criteria
May 3, 2023
First Posted (Estimate)
May 5, 2023
Study Record Updates
Last Update Posted (Estimate)
May 5, 2023
Last Update Submitted That Met QC Criteria
May 3, 2023
Last Verified
May 1, 2023
More Information
Terms related to this study
Other Study ID Numbers
- 3968
Plan for Individual participant data (IPD)
Plan to Share Individual Participant Data (IPD)?
UNDECIDED
Drug and device information, study documents
Studies a U.S. FDA-regulated drug product
No
Studies a U.S. FDA-regulated device product
No
This information was retrieved directly from the website clinicaltrials.gov without any changes. If you have any requests to change, remove or update your study details, please contact register@clinicaltrials.gov. As soon as a change is implemented on clinicaltrials.gov, this will be updated automatically on our website as well.
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