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Novel Imaging Techniques in Barrett's Esophagus
This study is currently recruiting participants.
Verified by Kansas City Veteran Affairs Medical Center, June 2008
Sponsors and Collaborators: Kansas City Veteran Affairs Medical Center
Medical University of South Carolina
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Information provided by: Kansas City Veteran Affairs Medical Center
ClinicalTrials.gov Identifier: NCT00576498
  Purpose

Primary Aim: In patients with endoscopically suspected BE, compared to standard endoscopy, novel techniques (NBI and AFI) with target biopsies will

  • Detect more patients with intestinal metaplasia
  • Detect more areas of high grade dysplasia
  • Require fewer biopsies and a shorter time for procedure completion

Secondary Aim:

  • Compare the yield of high-grade dysplasia(HGD)using NBI/AFI versus standard endoscopy with biopsy.
  • Compare the number of biopsies and procedure times for NBI/AFI versus standard endoscopy with biopsy.
  • Compare the inter-observer variability in classifying different mucosal and vascular patterns observed by NBI/AFI using kappa statistics.

Condition Intervention
Barrett Esophagus
Gastroesophageal Reflux
Other: NBI-AFI imaging
Other: Standard Endoscopy

MedlinePlus related topics: Endoscopy GERD
U.S. FDA Resources
Study Type: Interventional
Study Design: Diagnostic, Randomized, Double Blind (Subject, Investigator), Active Control, Crossover Assignment, Efficacy Study
Official Title: Detection Of Intestinal Metaplasia And High Grade Dysplasia In Barrett's Esophagus Using Novel Imaging Techniques - A Randomized Controlled Trial.

Further study details as provided by Kansas City Veteran Affairs Medical Center:

Primary Outcome Measures:
  • Proportion of patients with biopsy confirmed intestinal metaplasia [ Time Frame: 08/2006 to 10/2008 ] [ Designated as safety issue: No ]

Secondary Outcome Measures:
  • Detection of high grade dysplasia [ Time Frame: 08/2006 to 10/2008 ] [ Designated as safety issue: No ]
  • Procedure time [ Time Frame: 08/2006 to 10/2008 ] [ Designated as safety issue: No ]
  • Number of biopsies [ Time Frame: 08/2006 to 10/2008 ] [ Designated as safety issue: No ]
  • Inter observer variability in reading of mucosal and vascular patterns [ Time Frame: 08/2006 to 10/2008 ] [ Designated as safety issue: No ]

Estimated Enrollment: 130
Study Start Date: August 2006
Estimated Study Completion Date: October 2009
Estimated Primary Completion Date: September 2009 (Final data collection date for primary outcome measure)
Arms Assigned Interventions
1: Experimental

Narrow Band Imaging- Patients will be evaluated with a standard magnification endoscope (Olympus GIF Q240Z, 115x) using a NBI light source.

Autofluorescence Imaging- Patients will be evaluated using a prototype autofluorescence endoscope (Olympus, Tokyo, Japan; excitation 395-475 nm, fluorescence detection 490-625 nm, red reflectance 600-620 nm and green reflectance 540-560 nm)

Other: NBI-AFI imaging

Narrow Band Imaging- Patients will be evaluated with a standard magnification endoscope (Olympus GIF Q240Z, 115x) using a NBI light source.Target biopsies with standard biopsy forceps will be obtained from the different visualized patterns in separate jars.

Autofluorescence Imaging- Patients will be evaluated using a prototype autofluorescence endoscope (Olympus, Tokyo, Japan; excitation 395-475 nm, fluorescence detection 490-625 nm, red reflectance 600-620 nm and green reflectance 540-560 nm).In this system, normal squamous and non-dysplastic BE appears green while the dysplastic areas appear magenta/purplish. Targeted biopsies will be obtained from the areas with abnormal fluorescence.

2
Standard Endoscopy- Patients will undergo EGD with biopsies using a standard diagnostic video endoscope (Olympus, GIF 140 or 160) using the Seattle protocol - 4 quadrant biopsies using standard biopsy forceps every 2 cms; stored in separate jars
Other: Standard Endoscopy
Standard Endoscopy- Patients will undergo EGD with biopsies using a standard diagnostic video endoscope (Olympus, GIF 140 or 160) using the Seattle protocol - 4 quadrant biopsies using standard biopsy forceps every 2 cms; stored in separate jars.

  Show Detailed Description

  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Patients with suspected Barrett's esophagus on endoscopy
  • Age > 18 years
  • Ability to provide written informed consent

Exclusion Criteria:

  • Presence of erosive esophagitis
  • Visible nodules, lesions within Barrett's esophagus segment
  • Endoscopist aware of biopsy results
  • Inability to obtain biopsies due to anticoagulation or varices
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00576498

Contacts
Contact: April Higbee, RN 8168614700 ext 57456 april.higbee@va.gov

Locations
United States, Missouri
Veterans Affairs Medical Center Recruiting
Kansas city, Missouri, United States, 64128
Contact: April Higbee, RN     816-861-4700 ext 57456        
Sub-Investigator: Ajay Bansal, MD            
Sub-Investigator: Amit Rastogi, MD            
Sub-Investigator: Prashant Pandya, DO            
Sub-Investigator: Sharad Mathur, MD            
Principal Investigator: Prateek Sharma, MD            
Sub-Investigator: Sachin Wani, MD            
Sponsors and Collaborators
Kansas City Veteran Affairs Medical Center
Medical University of South Carolina
Academisch Medisch Centrum - Universiteit van Amsterdam (AMC-UvA)
Investigators
Principal Investigator: Prateek Sharma, MD Veterans Affairs Medical Center, Kansas City, MO; University of Kansas School of Medicine
  More Information

Publications:
Weinstein WM, Ippoliti AF. The diagnosis of Barrett's esophagus: goblets, goblets, goblets. Gastrointest Endosc. 1996 Jul;44(1):91-5. No abstract available.
Devesa SS, Blot WJ, Fraumeni JF Jr. Changing patterns in the incidence of esophageal and gastric carcinoma in the United States. Cancer. 1998 Nov 15;83(10):2049-53.
Brown LM, Devesa SS. Epidemiologic trends in esophageal and gastric cancer in the United States. Surg Oncol Clin N Am. 2002 Apr;11(2):235-56. Review.
Gerson LB, Shetler K, Triadafilopoulos G. Prevalence of Barrett's esophagus in asymptomatic individuals. Gastroenterology. 2002 Aug;123(2):461-7.
Rex DK, Cummings OW, Shaw M, Cumings MD, Wong RK, Vasudeva RS, Dunne D, Rahmani EY, Helper DJ. Screening for Barrett's esophagus in colonoscopy patients with and without heartburn. Gastroenterology. 2003 Dec;125(6):1670-7.
Hamilton SR, Smith RR, Cameron JL. Prevalence and characteristics of Barrett esophagus in patients with adenocarcinoma of the esophagus or esophagogastric junction. Hum Pathol. 1988 Aug;19(8):942-8.
Sampliner RE. Practice guidelines on the diagnosis, surveillance, and therapy of Barrett's esophagus. The Practice Parameters Committee of the American College of Gastroenterology. Am J Gastroenterol. 1998 Jul;93(7):1028-32. No abstract available.
Sharma P, McQuaid K, Dent J, Fennerty MB, Sampliner R, Spechler S, Cameron A, Corley D, Falk G, Goldblum J, Hunter J, Jankowski J, Lundell L, Reid B, Shaheen NJ, Sonnenberg A, Wang K, Weinstein W; AGA Chicago Workshop. A critical review of the diagnosis and management of Barrett's esophagus: the AGA Chicago Workshop. Gastroenterology. 2004 Jul;127(1):310-30. Review.
Eloubeidi MA, Provenzale D. Does this patient have Barrett's esophagus? The utility of predicting Barrett's esophagus at the index endoscopy. Am J Gastroenterol. 1999 Apr;94(4):937-43.
Inadomi JM, Sampliner R, Lagergren J, Lieberman D, Fendrick AM, Vakil N. Screening and surveillance for Barrett esophagus in high-risk groups: a cost-utility analysis. Ann Intern Med. 2003 Feb 4;138(3):176-86.
Cameron AJ, Carpenter HA. Barrett's esophagus, high-grade dysplasia, and early adenocarcinoma: a pathological study. Am J Gastroenterol. 1997 Apr;92(4):586-91.

Responsible Party: Kansas city VA Medical Center ( PRATEEK SHARMA )
Study ID Numbers: 00225(PS0036)
Study First Received: December 18, 2007
Last Updated: June 13, 2008
ClinicalTrials.gov Identifier: NCT00576498  
Health Authority: United States: Federal Government;   United States: Institutional Review Board

Keywords provided by Kansas City Veteran Affairs Medical Center:
GERD
NBI
AFI
IM
SSBE
LSBE
LGD
HGD

Study placed in the following topic categories:
Deglutition Disorders
Esophageal Motility Disorders
Digestive System Diseases
Digestive System Abnormalities
Esophageal disorder
Gastrointestinal Diseases
Metaplasia
Barrett Esophagus
Esophageal Diseases
Congenital Abnormalities
Gastroesophageal Reflux

ClinicalTrials.gov processed this record on January 16, 2009