Breast Cancer Clinical Trial

The Cancer of the Pancreas Screening-5 CAPS5)Study

Summary

Johns Hopkins clinical research office quality assurance group will monitor and audit this study at Johns Hopkins. The Sub Investigator at each site will be responsible for internal monitoring at their site.

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Full Description

The Sub Investigator at each site will be responsible for internal monitoring at their site. The site sub Investigator and study team will report any serious adverse events to Principal Investigator and annually report adverse events.

View Eligibility Criteria

Eligibility Criteria

Inclusion Criteria:

Hereditary Pancreatitis or
Peutz-Jeghers Syndrome or
Strong family history of pancreas cancer on one side of the family tree or
Confirmed germline mutation carrier (BRCA2, FAMMM, PALB2, BRCA1, HNPCC, PRSS1/2, or CTRC
Endoscopic evaluation of pancreas scheduled

Exclusion Criteria:

Medical comorbidities or coagulopathy that contraindicate endoscopy
Prior surgery that prevent optimal endoscopic ultrasound such as partial or complete gastrectomy with Bilroth or Roux-en-Y anastomosis
Stricture or obstruction in the upper GI tract that does not allow passage of the echoendoscope
Poor performance status
Inability to provide informed consent
Pregnancy.

Study is for people with:

Breast Cancer

Phase:

Phase 3

Estimated Enrollment:

7000

Study ID:

NCT02000089

Recruitment Status:

Recruiting

Sponsor:

Johns Hopkins University

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There are 8 Locations for this study

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Yale University
New Haven Connecticut, 06520, United States More Info
Scott Merenda, BSN
Contact
203-785-7019
[email protected]
James Farrell, MD
Principal Investigator
Johns Hopkins Hospital
Baltimore Maryland, 21287, United States More Info
Hilary Cosby, RN, CGRN
Contact
410-502-2893
[email protected]
Michael Goggins, MD
Principal Investigator
Marcia I Canto, MD
Sub-Investigator
Dana Farber Cancer Center, Harvard University
Boston Massachusetts, 02215, United States More Info
Emily Blair
Contact
617-632-4788
[email protected]
Chinedu Ukaegbu
Contact
[email protected]
Sapna Syngal, MD
Principal Investigator
University of Michigan
Ann Arbor Michigan, 48109, United States More Info
Erika Koeppe, MS
Contact
734-998-1274
[email protected]
Elena Stoffel, MD
Sub-Investigator
Columbia University Medical Center
New York New York, 10032, United States More Info
Tiffany Lam
Contact
[email protected]
Fay Kastrinos, MD
Principal Investigator
Case Comprehensive Cancer Center, Case Western Medical Reserve
Cleveland Ohio, 44106, United States More Info
Barbara Heaton
Contact
216-844-7314
[email protected]
Wendy Brock, RN
Contact
216-844-3853
[email protected]
Amitabh Chak, MD
Sub-Investigator
University of Pennsylvania
Philadelphia Pennsylvania, 19104, United States More Info
Maureen DeMarshall, RN
Contact
215-349-8546
[email protected]
Daniel Clay
Contact
[email protected]
Bryson Katona, MD
Sub-Investigator
University of Pittsburgh
Pittsburgh Pennsylvania, 15213, United States More Info
Christine Decapite
Contact
[email protected]
Nancy Abubaker
Contact
[email protected]
Randall Brand, MD
Principal Investigator

How clear is this clinincal trial information?

Study is for people with:

Breast Cancer

Phase:

Phase 3

Estimated Enrollment:

7000

Study ID:

NCT02000089

Recruitment Status:

Recruiting

Sponsor:


Johns Hopkins University

How clear is this clinincal trial information?

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