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Clinical Trials/NCT05714111
NCT05714111
Recruiting
Not Applicable

Radiology Registry on Pancreatic Malignancies

IRCCS San Raffaele1 site in 1 country1,300 target enrollmentMarch 4, 2022

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pancreatic Cancer
Sponsor
IRCCS San Raffaele
Enrollment
1300
Locations
1
Primary Endpoint
Progression- free survival
Status
Recruiting
Last Updated
2 years ago

Overview

Brief Summary

The purpose of this study is to collect all radiological data which evaluated with clinical data may help assess malignancy and prognosis of pancreatic disease.This registry aims to collect retrospective data from 2014 and prospective data until 2027 with a maximum follow-up of 3 years per patient.

Detailed Description

Single center, observational (retrospective and prospective) will collect all available parameters to assess the clinical outcome of the patients (progression free survival (PFS), overall survival (OS), local progression free survival LTPFS), response to treatment) with pancreatic neoplasms presenting to San Raffaele. Patient assignment to a given diagnostic and/or therapeutic procedure is not related to random assignment methods but is part of the ordinary therapeutic strategy planned for each patient on an individual basis and after multidisciplinary discussion.

Registry
clinicaltrials.gov
Start Date
March 4, 2022
End Date
March 30, 2030
Last Updated
2 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Francesco De Cobelli

Head of Radiology

IRCCS San Raffaele

Eligibility Criteria

Inclusion Criteria

  • ≥18 years of age
  • Patients with suspect (planned for investigation) or diagnosed pancreatic cancer at any stage.
  • able and willing to sign informed consent

Exclusion Criteria

  • Patients with non-primary pancreatic disease

Outcomes

Primary Outcomes

Progression- free survival

Time Frame: From date of intervention until the date of first documented progression, up to a maximum of 3 years

Time from start of observation to disease progression

Local progression free survival

Time Frame: From date of intervention until the date of first documented local progression assessed up to a maximum of 3 years

Time between (start of) a locoregional treatment and local disease progression

Secondary Outcomes

  • Overall Survival(From date of treatment until the date of death from any cause assessed up to 3 years)

Study Sites (1)

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