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Early Increase in Blood Flow (EIBS) in the Duodenum in Patients With Pancreatic Cancer


2010-06


2012-10


2012-10


37

Study Overview

Early Increase in Blood Flow (EIBS) in the Duodenum in Patients With Pancreatic Cancer

Pancreatic cancer is the fourth leading cause of cancer death in the United States and is associated with a poor prognosis. The average life expectancy after diagnosis is approximately 5 to 8 months. At present, successful surgical resection is the only curative therapy that can improve long-term survival. However, it can be achieved only when a tumor is detected at an early stage. Unfortunately, due to non-specific symptoms associated with pancreatic cancer, it is commonly detected in the later stages of the disease. The investigators hypothesized that pancreatic cancer could be detected by measuring the changes in the early increase in blood supply (EIBS) found in the surrounding normal-appearing duodenal tissue. The investigators tested a device called Four-dimensional Elastic Light-Scattering Fingerprinting (4D-ELF). The device used in this study is considered investigational, which means it has either not been approved by the Food and Drug Administration (FDA) for routine clinical use or for the use described in this study. However the FDA allowed the use of this device in this research study.

According to field effect theory, by detecting microvasculature changes in the early increase of blood supply in the surrounding tissue neoplastic lesions can be identified from a distance. The objective of this study was to determine the feasibility and efficacy of a fiberoptic probe containing novel Polarization Gating Spectroscopy (PGS) technology to identify patients with pancreatic adenocarcinoma (PAC) by field effect theory. EIBS markers, deoxyhemoglobin concentration (DHb), and average blood vessel radius (BVR) were evaluated in patients with PAC versus controls. During the subjects' esophagogastroduodenoscopy (EGD) with upper endoscopic ultrasound (EUS), the new optic probe was inserted inside the endoscope and advanced to the tip of the endoscope prior to the scope being withdrawn. As the scope was withdrawn, the light optic probe was used to examine approximately 5 sections of the small bowel: 1) directly on the ampulla, 2) approximately 5 mm proximal from the ampulla, 3) approximately 5 mm distal from the ampulla, 4) 1 cm proximal from the ampulla, and 5) 1 cm distal from the ampulla. Spectroscopy measurements were obtained four times in each of these five peri-ampullary locations. The rest of the EGD and upper EUS endoscopy procedures were then completed as clinically indicated. During the procedure, all visualized mucosal abnormalities were recorded and photographed.

  • Pancreatic Cancer
  • PROCEDURE: EGD with EUS
  • DEVICE: 4D-ELF
  • 09-002596
  • R01CA128641 (U.S. NIH Grant/Contract)
  • R01CA156186 (U.S. NIH Grant/Contract)
  • R01EB003682 (U.S. NIH Grant/Contract)
  • U01CA111257 (U.S. NIH Grant/Contract)
  • CBET-1240416 (OTHER_GRANT Identifier) (OTHER_GRANT: National Science Foundation)

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates Results Reporting Dates Study Record Updates

2009-11-12  

2014-05-29  

2014-07-03  

2009-11-17  

2014-05-29  

2014-07-16  

2009-11-18  

2014-07-02  

2014-07  

Study Plan

This section provides details of the study plan, including how the study is designed and what the study is measuring.

Design Details

Primary Purpose:
Diagnostic


Allocation:
Non Randomized


Interventional Model:
Parallel


Masking:
None


Arms and Interventions

Participant Group/ArmIntervention/Treatment
EXPERIMENTAL: Cancer group

Participants in this group had pathologically confirmed pancreatic adenocarcinoma. They received an EGD with EUS. During the EUS, blood flow was measured in the duodenum with the 4D-ELF device.

PROCEDURE: EGD with EUS

  • EUS was performed in order to measure blood flow in duodenum.

DEVICE: 4D-ELF

  • During the EUS, blood flow was measured in the duodenum with the 4D-ELF device.
OTHER: Control group

Participants in this group were without pancreatic adenocarcinoma. Participants in the control group received an EGD with EUS for the indication of abdominal pain. During the EUS, blood flow was measured in the duodenum with the 4D-ELF device.

PROCEDURE: EGD with EUS

  • EUS was performed in order to measure blood flow in duodenum.

DEVICE: 4D-ELF

  • During the EUS, blood flow was measured in the duodenum with the 4D-ELF device.
Primary Outcome MeasuresMeasure DescriptionTime Frame
Deoxyhemoglobin Concentration (DHb)Deoxygenated hemoglobin is the form of hemoglobin without the bound oxygen. It serves as a marker for early increase of blood supply (EIBS). DHb concentration was determined spectroscopically from five peri-ampullary locations.Completion of study procedure (endoscopic ultrasound), approximately 30 minutes from procedure initiation
Mean Blood Vessel Radius (BVR)BVR serves as a marker for early increase of blood supply (EIBS).Completion of study procedure (endoscopic ultrasound), approximately 30 minutes from procedure initiation
Secondary Outcome MeasuresMeasure DescriptionTime Frame

Contacts and Locations

This section provides the contact details for those conducting the study, and information on where this study is being conducted.

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person’s general health condition or prior treatments.

Ages Eligible for Study:
ALL

Sexes Eligible for Study:
18 Years

Accepts Healthy Volunteers:

    Inclusion Criteria:

  • Age 18 years or older.
  • Informed written consent.
  • Patient scheduled for previously planned EGD with upper EUS
  • Patients with known adenocarcinoma of the pancreas included in the cancer group
  • Patients with abdominal imaging studies (e.g., CT abdomen or MRI abdomen) negative for malignancy in past 5 years included in the control group.

  • Exclusion Criteria:

  • Unable to obtain biopsy specimen or fine-needle aspiration results of the pancreas lesion (e.g., coagulation disorder, inadequate sample)
  • Presence of malignant lesion in the pancreas or duodenum other than pancreas adenocarcinoma (e.g., neuroendocrine tumor, gastrointestinal stromal tumor)
  • Known familial disorder with high risk of pancreas cancer development (e.g., familial adenomatous polyposis syndrome, hereditary non-polyposis colorectal cancer syndrome, juvenile polyposis syndrome)
  • Significant family history of pancreatic cancer (at least one first degree relative with pancreatic cancer)
  • Presence of premalignant lesions (e.g., duodenal adenoma, pancreas intraductal papillary mucinous neoplasm)
  • Active visible inflammation/ulcer in the stomach or the duodenum
  • Patients with known chronic pancreatitis were excluded from cancer group. Chronic pancreatitis patients were allowed to be included in the control group only.
  • Known pregnancy or sexually active females of childbearing age who are not practicing an accepted form of birth control.

Collaborators and Investigators

This is where you will find people and organizations involved with this study.

  • Northwestern University
  • National Cancer Institute (NCI)
  • National Institute for Biomedical Imaging and Bioengineering (NIBIB)

  • PRINCIPAL_INVESTIGATOR: Michael B. Wallace, MD MPH, Mayo Clinic

Publications

The person responsible for entering information about the study voluntarily provides these publications. These may be about anything related to the study.

General Publications

  • Patel M, Gomes A, Ruderman S, Hardee D, Crespo S, Raimondo M, Woodward T, Backman V, Roy H, Wallace M. Polarization gating spectroscopy of normal-appearing duodenal mucosa to detect pancreatic cancer. Gastrointest Endosc. 2014 Nov;80(5):786-93.e1-2. doi: 10.1016/j.gie.2014.03.031. Epub 2014 May 24.