Viewing Study NCT03060720


Ignite Creation Date: 2025-12-25 @ 4:14 AM
Ignite Modification Date: 2026-01-29 @ 3:14 AM
Study NCT ID: NCT03060720
Status: ACTIVE_NOT_RECRUITING
Last Update Posted: 2025-03-14
First Post: 2017-02-15
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Systematic Hereditary Pancreatic Cancer Risk Assessment and Implications for Personalized Therapy
Sponsor: Dana-Farber Cancer Institute
Organization:

Study Overview

Official Title: Systematic Hereditary Pancreatic Cancer Risk Assessment and Implications for Personalized Therapy
Status: ACTIVE_NOT_RECRUITING
Status Verified Date: 2025-03
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: This research study is looking at people with cancer of the pancreas to find clinical factors that can explain the presence of genetic mutations
Detailed Description: This research is being done to identify which pancreatic cancer patients should undergo genetic evaluation. A patient's personal and family history of cancer is the information typically used to make this decision, but there are currently no accurate, evidence-based guidelines that exist to help doctors use this information to make a decision.

The investigators hope that by testing all new pancreatic cancer patients, they can determine which clinical factors predict for genetic mutations in order to create a risk assessment tool.

The investigators want to determine which patients with pancreatic cancer will benefit from genetic testing. To do so, the investigators will offer all patients with pancreatic cancer in the Dana-Farber Gastrointestinal Oncology clinic referral for genetic evaluation. At the Cancer Genetics and Prevention clinic appointment, the provider will review the patient's personal and familial history of cancer and offer genetic testing.

Study Oversight

Has Oversight DMC: True
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
P50CA127003 NIH None https://reporter.nih.gov/quic… View