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Clinical Trials/NCT06552078
NCT06552078
Recruiting
Not Applicable

Activation of Biobank for Association Study Between Environmental and Genetic Factors in Inflammatory, Functional and Neoplastic Bilio-pancreatic Diseases

IRCCS San Raffaele1 site in 1 country2,000 target enrollmentJune 9, 2021

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Pancreatitis
Sponsor
IRCCS San Raffaele
Enrollment
2000
Locations
1
Primary Endpoint
The rate of patients with each pancreatic disorder presenting with certain exposures or certain biomarkers
Status
Recruiting
Last Updated
last year

Overview

Brief Summary

The purpose of establishing the biobank is to create a collection of biological material and clinical data, with a prospective and retrospective mold, in order to investigate the role of genetic predisposition in multifactorial bilio-pancreatic diseases, so that an evaluation of the possible association in the pathogenesis of exogenous factors with endogenous factors can be allowed.

Multifactorial diseases are in fact an expression of genetic predisposition upon which one or more environmental stimuli act. Usually the aforementioned factors are not capable individually of triggering disease but, when simultaneously present, can cause the pathological phenotype. Therefore, it becomes important in the description of disease pathogenesis to identify as many risk factors for disease prevention and early diagnosis.

Detailed Description

Samples collected depending on the disease: * Peripheral blood; * Portal blood; * Saliva; * Urine; * Stool; * Cystic fluid; * Pancreatic juice; * Biopsy tissue specimens;

Registry
clinicaltrials.gov
Start Date
June 9, 2021
End Date
December 31, 2030
Last Updated
last year
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Paolo Giorgio Arcidiacono, MD

Professor

IRCCS San Raffaele

Eligibility Criteria

Inclusion Criteria

  • age \>= 18 years
  • signed informed consent

Exclusion Criteria

  • age \< 18 years
  • unwilling to sign informed consent

Outcomes

Primary Outcomes

The rate of patients with each pancreatic disorder presenting with certain exposures or certain biomarkers

Time Frame: Tthrough study completion, an average of 1 year

The rate of patients with each pancreatic disorder presenting with certain exposures or certain biomarkers will be evaluated by descriptive statistics and when available compared with that of subjects without such disorders (controls).

Study Sites (1)

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