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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT02000089
Other study ID # NA_00087754
Secondary ID 1U01CA210170-01R
Status Recruiting
Phase Phase 3
First received
Last updated
Start date January 6, 2014
Est. completion date December 2025

Study information

Verified date March 2024
Source Johns Hopkins University
Contact Hilary Cosby, RN
Email hcosby1@jhmi.edu
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial 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.


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.


Recruitment information / eligibility

Status Recruiting
Enrollment 7000
Est. completion date December 2025
Est. primary completion date October 2024
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility 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 Design


Intervention

Drug:
Secretin
inject Secretin to stimulate pancreatic digestive fluid, which is collected in duodenum near ampulla via endoscope suction port. This fluid will be assessed for biomarkers.
Diagnostic Test:
MRI
MRI abdomen with contrast (MRCP) will be clinically indicated for abnormal novel CA-19-9 lab results.
Other:
Tumor marker gene test with CA19-9
A tumor marker gene test that will be used to stratify individuals into one of several circulating tumor marker reference ranges for CA19-9. The variants in the genes FUT3 and FUT2 affect the levels of CA19-9.

Locations

Country Name City State
United States University of Michigan Ann Arbor Michigan
United States Johns Hopkins Hospital Baltimore Maryland
United States Dana Farber Cancer Center, Harvard University Boston Massachusetts
United States Case Comprehensive Cancer Center, Case Western Medical Reserve Cleveland Ohio
United States Yale University New Haven Connecticut
United States Columbia University Medical Center New York New York
United States University of Pennsylvania Philadelphia Pennsylvania
United States University of Pittsburgh Pittsburgh Pennsylvania

Sponsors (4)

Lead Sponsor Collaborator
Johns Hopkins University ChiRhoClin, Inc., National Cancer Institute (NCI), National Institutes of Health (NIH)

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Other Time disease progression and prevalence Aim #3: To determine the prevalence of pancreatic lesions, pancreatic fluid mutations and circulating pancreatic epithelial cells among a large cohort of high-risk individuals undergoing pancreatic screening and surveillance of a new cohort in which screening is begun at age >55. 10 years
Other Diagnostic performance of a tumor marker gene test for CA19-9 interpretation Aim #4 To evaluate the diagnostic performance of a tumor marker gene test to personalize the normal reference range of tumor markers such as CA19-9 for patients undergoing pancreatic surveillance. 5 years
Primary Evaluate pancreatic juice for early cancer markers. Aim #1: To evaluate pancreatic fluid mutations and circulating pancreatic epithelial cells as accurate markers of neoplasia by comparing their prevalence in cases with sporadic pancreatic neoplasia to healthy and disease controls. 10 years
Secondary Compare pancreas juice with pancreas cyst fluid Aim #2: To compare the prevalence of pancreatic fluid mutations and circulating pancreatic epithelial cells among a prospective cohort of individuals with sporadic pancreatic cysts undergoing pancreatic surveillance. 10 years
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