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Confocal Laser Endomicroscopy for the Diagnosis of Gastric Intestinal Metaplasia, Intraepithelial Neoplasia, and Carcinoma

Primary Purpose

Gastric Intestinal Metaplasia, Gastric Intraepithelial Neoplasia, Gastric Carcinoma

Status
Unknown status
Phase
Not Applicable
Locations
International
Study Type
Interventional
Intervention
Confocal laser endomicroscopy (Pentax, EG3870K)
Standard White-light endoscopy (Pentax, 90i)
Sponsored by
Shandong University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Gastric Intestinal Metaplasia focused on measuring confocal laser endomicroscopy, gastric intestinal metaplasia, gastric intraepithelial neoplasia, gastric carcinoma

Eligibility Criteria

18 Years - 80 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Male or Female aged 18-80
  • Patients with H. pylori infection, or histologically verified gastric intestinal metaplasia, low-grade intraepithelial neoplasia, and atrophic gastritis

Exclusion Criteria:

  • Patients with gastrectomy, acute GI bleeding, and advanced gastric cancer
  • Patients under conditions unsuitable for performing CLE including coagulopathy, impaired renal function, pregnancy or breastfeeding, and known allergy to fluorescein sodium
  • Inability to provide informed consent and other situations that could interfere with the examination protocol

Sites / Locations

  • the University of New South Wales, Bankstown-Lidcombe Hospital
  • the Prince of Wales Hospital, Chinese University of Hong Kong
  • Qilu Hospital, Shandong University
  • National University Hospital, National University of Singapore

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Experimental

Arm Label

CLE-TB

WLE-SB

Arm Description

Confocal laser endomicroscopy with Targeted Biopsy

Standard White-light endoscopy with Standard Biopsy

Outcomes

Primary Outcome Measures

number of participant with gastric IM/IN/CA
To determine whether CLE with optical biopsy and targeted mucosal biopsy improves the diagnostic yield of gastric IM/IN/CA in high risk populations compared to WLE with standard biopsy protocol.

Secondary Outcome Measures

number of biopsies needed per patient
To determine whether CLE with optical biopsy and targeted biopsy, as compared to WLE with standard biopsy, can reduce the number of biopsies needed per patient for detection of gastric IM/IN/CA without the loss of corresponding diagnostic yield.

Full Information

First Posted
July 11, 2012
Last Updated
July 17, 2012
Sponsor
Shandong University
Collaborators
Prince of Wales Hospital, Shatin, Hong Kong, National University Hospital, Singapore, The University of New South Wales
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1. Study Identification

Unique Protocol Identification Number
NCT01642797
Brief Title
Confocal Laser Endomicroscopy for the Diagnosis of Gastric Intestinal Metaplasia, Intraepithelial Neoplasia, and Carcinoma
Official Title
Confocal Laser Endomicroscopy for the Diagnosis of Gastric Intestinal Metaplasia, Intraepithelial Neoplasia, and Carcinoma: A Multicenter, Randomized, Controlled Trial
Study Type
Interventional

2. Study Status

Record Verification Date
July 2012
Overall Recruitment Status
Unknown status
Study Start Date
August 2012 (undefined)
Primary Completion Date
August 2013 (Anticipated)
Study Completion Date
September 2013 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Shandong University
Collaborators
Prince of Wales Hospital, Shatin, Hong Kong, National University Hospital, Singapore, The University of New South Wales

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
i. To determine whether Confocal Laser Endomicroscopy (CLE) with optical biopsy and targeted mucosal biopsy improves the diagnostic yield of gastric IM/IN/CA in high risk populations compared to WLE with standard biopsy protocol. ii. To determine whether CLE with optical biopsy and targeted biopsy, as compared to WLE with standard biopsy, can reduce the number of biopsies needed per patient for detection of gastric IM/IN/carcinoma without the loss of corresponding diagnostic yield. iii. To compare the sensitivity and specificity of CLE with WLE for the detection of gastric IM/IN/CA.
Detailed Description
Gastric cancer remains the world's second leading cause of cancer-related deaths. The prognosis for patients with this cancer clearly depends on stage at diagnosis. At least for the intestinal subtype of gastric adenocarcinoma, a cascade of histopathologic lesions has been defined: chronic gastritis, atrophic chronic gastritis, intestinal metaplasia (IM), and intraepithelial neoplasia (IN). The identification of these lesions and follow-up of patients in whom they are found could lead to diagnosis of gastric cancer at an early stage, thus improving patients' survival. The diagnosis of these lesions, which often appear in flat mucosa, is currently based on histopathologic examination of endoscopic biopsy specimens. However, conventional white-light endoscopy (WLE) for this purpose has high interobserver variability and a poor correlation with histopathologic finding. Confocal laser endomicroscopy (CLE), producing both conventional WLE and confocal microscopic images, can provide a direct histological observation of the in vivo tissue without the need for biopsy. Recently, CLE has shown its value for diagnosing gastric IM, intraepithelial neoplasia and carcinoma. However, none of those CLE criteria for gastric IM, IN or carcinoma (CA) has been validated in various endoscopic centers, hence reducing the reliability and clinical application of them.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Gastric Intestinal Metaplasia, Gastric Intraepithelial Neoplasia, Gastric Carcinoma
Keywords
confocal laser endomicroscopy, gastric intestinal metaplasia, gastric intraepithelial neoplasia, gastric carcinoma

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
242 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
CLE-TB
Arm Type
Experimental
Arm Description
Confocal laser endomicroscopy with Targeted Biopsy
Arm Title
WLE-SB
Arm Type
Experimental
Arm Description
Standard White-light endoscopy with Standard Biopsy
Intervention Type
Device
Intervention Name(s)
Confocal laser endomicroscopy (Pentax, EG3870K)
Intervention Description
Confocal laser endomicroscopy with Targeted Biopsy
Intervention Type
Device
Intervention Name(s)
Standard White-light endoscopy (Pentax, 90i)
Intervention Description
Standard White-light endoscopy with Standard Biopsy
Primary Outcome Measure Information:
Title
number of participant with gastric IM/IN/CA
Description
To determine whether CLE with optical biopsy and targeted mucosal biopsy improves the diagnostic yield of gastric IM/IN/CA in high risk populations compared to WLE with standard biopsy protocol.
Time Frame
1 year
Secondary Outcome Measure Information:
Title
number of biopsies needed per patient
Description
To determine whether CLE with optical biopsy and targeted biopsy, as compared to WLE with standard biopsy, can reduce the number of biopsies needed per patient for detection of gastric IM/IN/CA without the loss of corresponding diagnostic yield.
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
80 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or Female aged 18-80 Patients with H. pylori infection, or histologically verified gastric intestinal metaplasia, low-grade intraepithelial neoplasia, and atrophic gastritis Exclusion Criteria: Patients with gastrectomy, acute GI bleeding, and advanced gastric cancer Patients under conditions unsuitable for performing CLE including coagulopathy, impaired renal function, pregnancy or breastfeeding, and known allergy to fluorescein sodium Inability to provide informed consent and other situations that could interfere with the examination protocol
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Yanqing Li, PhD. MD.
Phone
86-531-8216923
Ext
82169508
Email
qiluliyanqign@gmail.com
Facility Information:
Facility Name
the University of New South Wales, Bankstown-Lidcombe Hospital
City
Bankstown
Country
Australia
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Rupert W. L. Leong, MD. PhD.
First Name & Middle Initial & Last Name & Degree
Rupert W Leong, MD. PhD.
Facility Name
the Prince of Wales Hospital, Chinese University of Hong Kong
City
Hongkong
State/Province
Hongkong
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joseph Jao-Yiu Sung, MD. PhD.
First Name & Middle Initial & Last Name & Degree
Joseph Jao-Yiu Sung, MD. PhD.
Facility Name
Qilu Hospital, Shandong University
City
Jinan
State/Province
Shandong
ZIP/Postal Code
20012
Country
China
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Yanqing Li, MD. PhD.
Facility Name
National University Hospital, National University of Singapore
City
Singapore
Country
Singapore
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Ho Khek Yu, MD. PhD.
First Name & Middle Initial & Last Name & Degree
Ho Khek Yu, MD. PhD.

12. IPD Sharing Statement

Learn more about this trial

Confocal Laser Endomicroscopy for the Diagnosis of Gastric Intestinal Metaplasia, Intraepithelial Neoplasia, and Carcinoma

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