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

Not Applicable

• Conditions: Gastric Intestinal Metaplasia; Gastric Intraepithelial Neoplasia; Gastric Carcinoma
• Interventions: Device: Confocal laser endomicroscopy (Pentax, EG3870K); Device: Standard White-light endoscopy (Pentax, 90i)

• Registration Number: NCT01642797
• Lead Sponsor: Shandong University

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.

Study Timeline

• Status Verified: 2012-07
• Study First Submitted: 2012-07-11
• Study First Submitted QC: 2012-07-16
• Study First Posted: 2012-07-17
• Last Update Submitted: 2012-07-17
• Last Update Posted: 2012-07-18
• Study Start: 2012-08
• Primary Completion: 2013-08
• Study Completion: 2013-09

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 242

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

Study & Design

• Study Type: INTERVENTIONAL
• Study Design: PARALLEL

Arm && Interventions

Group	Intervention	Description
CLE-TB	Confocal laser endomicroscopy (Pentax, EG3870K)	Confocal laser endomicroscopy with Targeted Biopsy
WLE-SB	Standard White-light endoscopy (Pentax, 90i)	Standard White-light endoscopy with Standard Biopsy

Primary Outcome Measures

Name	Time	Method
number of participant with gastric IM/IN/CA	1 year	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

Name	Time	Method
number of biopsies needed per patient	1 year	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.

Trial Locations

Locations (4)

National University Hospital, National University of Singapore; 🇸🇬 Singapore, Singapore

the Prince of Wales Hospital, Chinese University of Hong Kong; 🇨🇳 Hongkong, Hongkong, China

Qilu Hospital, Shandong University; 🇨🇳 Jinan, Shandong, China

the University of New South Wales, Bankstown-Lidcombe Hospital; 🇦🇺 Bankstown, Australia