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NCT03060720Active, not recruiting

Systematic Hereditary Pancreatic Cancer Risk Assessment and Implications for Personalized Therapy

Source: ClinicalTrials.gov · Last updated 30 Mar 2026

Brief summary (registry, in English)

This research study is looking at people with cancer of the pancreas to find clinical factors that can explain the presence of genetic mutations

Status (registry)
Active, not recruiting
Study type
Observational
Enrollment
271 (actual)
First submitted
15 Feb 2017
Start date
24 Feb 2017
Primary completion date
7 Apr 2019
Lead sponsor
Dana-Farber Cancer Institute
NCT number
NCT03060720

What you commit to

  • Study type: Observational
  • Participants enrolled: 271
  • From 24 Feb 2017 to the primary completion date, 7 Apr 2019
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other

  • Prospective participant unable to sign informed consent based on referring physician recommendation.
  • Patient has neuroendocrine pancreatic tumor

Who the study is looking for

  • Diagnosis of pancreatic ductal adenocarcinoma
  • Signed initial informed consent
  • Participant agrees to genetic counseling

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Dana-Farber Cancer Institute
Coordinator of this site? Confirm its status
BostonUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.