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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01662609
Other study ID # MCC-14882
Secondary ID
Status Completed
Phase
First received
Last updated
Start date August 23, 2007
Est. completion date August 16, 2022

Study information

Verified date October 2022
Source H. Lee Moffitt Cancer Center and Research Institute
Contact n/a
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

The purpose of this study is to find out whether Endoscopic Ultrasound (EUS) can detect early stage pre-cancerous or cancerous changes in the pancreas in patients at high-risk for the development of pancreatic cancer. Endoscopic refers to the use of an instrument called an endoscope - a thin, flexible tube with a tiny video camera and light on the end. Ultrasound refers to an imaging technique that uses sound waves to produce pictures. EUS in this research study is a method of combining endoscopy and ultrasound imaging to obtain high quality images of the pancreas.


Recruitment information / eligibility

Status Completed
Enrollment 90
Est. completion date August 16, 2022
Est. primary completion date August 16, 2022
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 30 Years and older
Eligibility Inclusion Criteria: - Patients will be eligible if they have 2 or more relatives with pancreatic cancer and have a first degree relationship with at least one of the relatives with pancreatic cancer - If only 2 family members are affected then both must have had pancreatic cancer and a first-degree relationship with individual screened - If there are more than 2 affected individuals on the same side of the family at least one of the individuals must have a first-degree relationship with the member being screened - Patients at least 40 years old or 10 years younger than the youngest affected individual - Peutz-Jeghers Syndrome (PJS) patients age>30 - Hereditary pancreatitis patients - Patients with Familial Atypical Multiple Mole Melanoma Syndrome (FAMMM) - Patients with BRCA2 mutation and at least one first or second degree relative with documented pancreatic cancer - Willingness to undergo (EUS) with possible Fine Needle Aspiration (FNA) - Willingness to undergo surgical evaluation for abnormal EUS/FNA finding - Willingness to undergo radiographic evaluation if screening findings are abnormal Exclusion Criteria: - Medical contraindications to undergoing endoscopy or obstruction of the GI tract that precludes passage of the endoscope - Personal history of pancreatic adenocarcinoma - Previous partial or complete resection of the pancreas for adenocarcinoma - Prior partial or total gastrectomy with Billroth II or Roux-en-Y anastamosis - Previous computed tomography (CT) scan, magnetic resonance imaging/magnetic resonance cholangiopancreatography (MRI/MRCP) or EUS of the abdomen in the past 3 years - Coexisting cancer in other organs or acquired immunodeficiency syndrome/human immunodeficiency virus (AIDS/HIV) - Life expectancy less than 5 years - Pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Procedure:
Endoscopic Ultrasound (EUS)
Ultrasound scope will be passed through the participant's mouth into their stomach and their pancreas will be evaluated completely by the ultrasound scope. If an abnormality is found in their pancreas, a biopsy may be performed to obtain a diagnosis.

Locations

Country Name City State
United States Lehigh Valley Health Network Allentown Pennsylvania
United States H. Lee Moffitt Cancer Center and Research Institute Tampa Florida

Sponsors (1)

Lead Sponsor Collaborator
H. Lee Moffitt Cancer Center and Research Institute

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Number of Abnormalities Detected by EUS To determine whether targeted screening of these high-risk individuals using Endoscopic Ultrasound (EUS) at regular intervals can detect precancerous pancreas changes or early stage asymptomatic pancreatic cancer. Average of 5 years
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