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临床试验/NCT02207959
NCT02207959终止1 期

Endoscopic Multispectral Imaging for the Early Detection of Gastric Neoplasia

Susana Gonzalez1 个研究点 分布在 1 个国家目标入组 8 人开始时间: 2015年1月最近更新:
适应症
干预措施
相关药物

试验速览

阶段
1 期
状态
终止
发起方
入组人数
8
试验地点
1
主要终点
Gastric neoplasia presence

研究概览

简要总结

The overall objective of this pilot study is to determine whether multispectral imaging increases the diagnostic accuracy of the current standard of high-definition white-light endoscopy for the detection of gastric neoplasia (high grade dysplasia or cancer). As part of an NCI-funded RO1, the investigators goal is to develop a multispectral endoscopic platform that can be used to survey a large surface area and, potentially, serve as a "red flag" for microendoscopic imaging of small areas. In prior ex vivo evaluations of surgical and endoscopic specimens, the investigators have identified the optical settings and illumination wavelengths that are complementary to white-light imaging and enhance superficial mucosal and vascular changes associated with neoplasia. Based on this initial testing, vital-dye enhanced fluorescence imaging (VFI) and imaging with High Resolution Microendoscope (HRME) have been identified as modalities that may be complementary to white-light imaging. The goal of this pilot study is to preliminarily determine the accuracy of these modalities during the endoscopic surveillance and detection of gastric neoplasia.

详细描述

Consent will be obtained the day of the subject's scheduled endoscopy in a clinical room or at a routine office visit prior to the endoscopy. The study investigator will explain the study including the reasons why subject may be eligible, risks, and benefits. The subject will be given a chance to address any questions or concerns they may have.

If the patient agrees to participate in this study all of the procedures listed below will be performed the day of the scheduled endoscopy exam. The procedures listed are part of the routine standard of care for an endoscopy exam, except for the images that are being taken and the additional 2-6 biopsies taken from any abnormal areas that are seen with the new imaging technique. The use of the imaging technique described in this research study will not change the standard of care procedures.

The endoscopic procedure is outlined below:

  1. White Light Examination: Examination will initially be performed in the standard white-light endoscopic mode as is routinely done. Abnormal gastric mucosa areas and nodularities will be recorded. Any "Suspicious" areas (visible abnormalities, etc.) will be photographed and the location recorded (distance from incisors and endoscopic quadrant, eq. 34 cm; greater curvature, lesser curvature, etc).
  2. Vital-Dye Enhanced Fluorescence Examination: Following this, the stomach will be sprayed with 1-10 ml of 0.01% proflavine using a standard endoscopic spray-catheter. Using the fluorescent imaging, the location of any VFI-"Suspicious' areas will be recorded. Additionally, VFI examination of any suspicious areas seen on WLE will be performed. The endoscopist will label the surface-appearance of each WLE abnormal area based on its VFI appearance. Thus, each area will be labeled as: "Not Suspicious," or "Suspicious for Neoplasia."
  3. HRME examination: WLE and VFI suspicious appearing areas will be further imaged with HRME. HRME will be inserted through the biopsy channel of the endoscope, gently placed against the mucosa, and images of suspicious areas will be obtained. The endoscopist will label the surface-appearance of each WLE abnormal area and VFI abnormal area, based on the HRME appearance. Thus, each area will be labeled as: "Not Suspicious," or "Suspicious for Neoplasia."
  4. Biopsy Protocol: Biopsies will be obtained of any area suspicious on any of the imaging modalities (WLE, VFI or HRME). Additionally, two 'control' areas (normal on imaging) will also be biopsied. Lastly, routine, biopsies will be performed per clinical care to determine areas of intestinal metaplasia and H pylori infection as per routine standard of care.
  5. Pathologic Interpretation: All samples will be evaluated by a single expert gastrointestinal pathologist who will be blinded to the endoscopic findings

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Diagnostic
盲法
None

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • patients with high grade dysplasia in the stomach and known or suspected cancer of the stomach undergoing endoscopic surveillance
  • at least 18 years of age

排除标准

  • subjects who report an allergy to Proflavine

研究组 & 干预措施

Surveillance Endoscopy

Experimental

White light examination, vital-dye enhanced fluorescence examination (VFI), High Resolution Microendoscope (HRME)

干预措施: Proflavine Hemisulphate salt (Drug)

Surveillance Endoscopy

Experimental

White light examination, vital-dye enhanced fluorescence examination (VFI), High Resolution Microendoscope (HRME)

干预措施: White-light examination (Procedure)

Surveillance Endoscopy

Experimental

White light examination, vital-dye enhanced fluorescence examination (VFI), High Resolution Microendoscope (HRME)

干预措施: Imaging with High Resolution Microendoscope (Procedure)

结局指标

主要结局

Gastric neoplasia presence

时间窗: Day 1

Comparison of the efficiency of widefield imaging modality or combination of modalities (WLE, WLE+VFI/HRME for the highest accuracy on the detection of gastric neoplasia

次要结局

  • Sensitivity for the detection of neoplasia(Day 1)
  • Specificity for the detection of neoplasia(Day 1)

研究者

发起方
Susana Gonzalez
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Susana Gonzalez

Assistant Professor

Icahn School of Medicine at Mount Sinai

研究点 (1)

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