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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT05714111
Other study ID # RadonPams
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date March 4, 2022
Est. completion date March 30, 2030

Study information

Verified date April 2024
Source IRCCS San Raffaele
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 1300
Est. completion date March 30, 2030
Est. primary completion date March 30, 2027
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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

Study Design


Intervention

Other:
Radiology evaluations and interventions
Diagnostic and interventional radiology procedures

Locations

Country Name City State
Italy Department of Radiology, IRCCS Ospedale San Raffaele Milan

Sponsors (1)

Lead Sponsor Collaborator
IRCCS San Raffaele

Country where clinical trial is conducted

Italy, 

Outcome

Type Measure Description Time frame Safety issue
Primary Progression- free survival Time from start of observation to disease progression From date of intervention until the date of first documented progression, up to a maximum of 3 years
Primary Local progression free survival Time between (start of) a locoregional treatment and local disease progression From date of intervention until the date of first documented local progression assessed up to a maximum of 3 years
Secondary Overall Survival The length of time from either the date of diagnosis or the start of treatment for a disease, in which the patients are still alive From date of treatment until the date of death from any cause assessed up to 3 years
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