Italian Registry of Families At Risk of Pancreatic Cancer

Status: Recruiting
Location: See all (4) locations...
Intervention Type: Procedure, Radiation
Study Type: Observational
SUMMARY

IRFARPC is a multicenter national registry designed to study the diagnosis and predisposing factors of subjects with an inherited increased risk for pancreatic cancer.

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Maximum Age: 80
View:

• individuals with at least two relatives suffering from pancreatic cancer, with at least 1 first-degree and until the third-degree

• subjects with known genetic mutation of BRCA2, BRCA1, p16, PALB2 with at least 1 first- or 2nd-degree relative suffering from pancreatic cancer

• subjects suffering from FAMMM Syndrome

• subjects suffering from Peutz-Jeghers Syndrome

• subjects suffering from PRSS-1- or CFTR- or SPINK-1- related pancreatitis

• subjects suffering from Lynch syndrome with at least 1 first- or 2nd-degree relative suffering from pancreatic cancer

• 45 years or 10 years younger than the youngest index case of pancreatic cancer in the family for familial cases

• 40 years or 5 years younger than the youngest index case of pancreatic cancer for subjects suffering from hereditary/genetic pancreatitis, Lynch syndrome, or carrying a known BRCA 1/2, PALB2, p16 genetic mutation with familiarity for pancreatic cancer

• 30 years for subjects suffering from FAMMM, Peutz-Jeghers syndrome

Locations
Other Locations
Italy
San Raffele Vita Salute University Hospital
RECRUITING
Milan
Ospedale Pederzoli
RECRUITING
Peschiera Del Garda
Istituto Clinico Humanitas
RECRUITING
Rozzano
Chirurgia Generale e del Pancreas
RECRUITING
Verona
Contact Information
Primary
Salvatore Paiella, MD, PhD
salvatore.paiella@univr.it
00390458126009
Backup
Silvia Carrara, MD
silvia.carrara@humanitas.it
+ 39 02 82247288
Time Frame
Start Date: 2019-08-20
Estimated Completion Date: 2045-09-20
Participants
Target number of participants: 1000
Treatments
Familial pancreatic cancer relatives
Peutz-Jeghers syndrome
BRCA 1/2, PALB2, p16 mutations with familiarity for PC
Known genetic mutation and at least 1 1st- or 2nd-degree relative suffering from PC
Lynch syndrome with familiarity for pancreatic cancer
FAMMM syndrome
Hereditary and genetic pancreatitis
Sponsors
Leads: Associazione Italiana per lo Studio del Pancreas

This content was sourced from clinicaltrials.gov