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Feasibility of Multi-Spectral Endoscopic Imaging for Detection of Early Neoplasia in Barrett's Oesophagus (MuSE)

Primary Purpose

Barrett Esophagus, Esophageal Neoplasms, Reflux Esophagitis

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Endoscopy with Polyscope (Polydiagnost TM) coupled with Multi-Spectral Imaging light-source
Sponsored by
University of Cambridge
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional device feasibility trial for Barrett Esophagus focused on measuring Barrett Esophagus, Endoscopy, Adenocarcinoma

Eligibility Criteria

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

Inclusion Criteria:

  • Male or female subjects over 18 years
  • Previous diagnosis of Barrett's oesophagus, with an endoscopic length of at least 2 cm
  • Previous diagnosis of oesophageal glandular dysplasia or early oesophageal adenocarcinoma for consideration of endoscopic therapy

Exclusion Criteria:

  • History of oesophageal stricture precluding passage of the endoscope,
  • Pregnancy, or planned pregnancy during the course of the study,
  • Currently breastfeeding
  • Any history of esophageal varices, liver impairment of moderate or worse severity (Child's- Pugh class B & C) or evidence of varices on initial treatment endoscopy,
  • Any history of oesophageal surgery, except for uncomplicated fundoplication, and,
  • History of coagulopathy, with INR>1.3 and/or platelet count of <75,000.
  • On clopidogrel, and/or warfarin for high risk condition and unable to withhold temporarily the medication.

Sites / Locations

  • MRC Cancer Unit

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Barrett's Esophagus patients

Arm Description

Multi-Spectral Endoscopic Imaging

Outcomes

Primary Outcome Measures

Level of confidence in delineating the area of interest by multispectral imaging
Level of confidence in delineating the area of interest by the multispectral endoscope in terms of image quality and visibility of area of interest assessed by endoscopist using a 1 to 10 Visual Analogue Score (VAS). We will consider the following ranges 0-3 poor; 4-5 fair; 6-8 good, 9-10 excellent

Secondary Outcome Measures

Imaging spectra by multispectral endoscopy in neoplastic vs. non-neoplastic Barrett's
Number and type of image spectra corresponding to neoplastic and non-neoplastic area of Barrett's Oesophagus
Patient comfort
Patient comfort score measured by assisting nurse according to standard scoring scale (1 to 5)
Time
Time to perform multispectral imaging in minutes
Correlation with molecular biomarkers
Comparison of the biomarker features of biopsies directed by multispectral imaging (both neoplastic and non-neoplastic) using a molecular panel assessing aneuploidy, p53 and cyclin A.

Full Information

First Posted
November 23, 2017
Last Updated
April 26, 2021
Sponsor
University of Cambridge
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1. Study Identification

Unique Protocol Identification Number
NCT03388047
Brief Title
Feasibility of Multi-Spectral Endoscopic Imaging for Detection of Early Neoplasia in Barrett's Oesophagus
Acronym
MuSE
Official Title
Prospective Pilot Cohort Study to Assess Feasibility of Multi-Spectral Endoscopic Imaging for Detection of Early Neoplasia in Barrett's Oesophagus
Study Type
Interventional

2. Study Status

Record Verification Date
April 2021
Overall Recruitment Status
Completed
Study Start Date
January 1, 2018 (Actual)
Primary Completion Date
December 31, 2020 (Actual)
Study Completion Date
December 31, 2020 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
University of Cambridge

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
Yes

5. Study Description

Brief Summary
Multispectral imaging represents an exciting new field of investigation in endoscopic research. Multispectral imaging uses a specialised camera to detect multiple colours, allowing us to build a rough spectrum from each point in our image. It is widely reported that these spectra are different for different tissue types, but this is difficult to study ex vivo since de-oxygenation of the blood and decay of the tissue change these spectra considerably. The investigators have therefore designed this study to asses the different multispectral imaging spectra of Barrett's Oesophagus, which we believe might be utilised as a method to detect dysplasia in the future.
Detailed Description
The investigators have developed a custom multispectral endoscopes based around a CE marked device, the PolyScope disposable endoscope (PolyDiagnost). This is a combined sterile catheter and fibre optic device designed to optimize light delivery to the anatomy and to acquire and transmit endoscopic images back to a camera. This CE marked system can be used to endoscope luminal organs such as the oesophagus, but also biliary tract, the bladder and the oro-pharynx. The PolyScope can be inserted thought the accessory channel of commercial endoscopes. The design of the fibre optic device is durable and re-useable; it is inserted within the disposable sterile catheter channel, which is able to flex and bend to orient the device to the region of interest for imaging. The fibre optic device never comes into contact with the patient. The sterile catheter, which shields the fibre optic device, is disposed following a procedure. The use of the PolyScope provides the advantage of building on a known system. The commercial PolyScope probe is coupled outside of the patient to a custom multispectral detection and illumination system. No modified part of the device comes into contact with the patient. The patients recruited to this study will have a clinical indication to an endoscopic examination for Barrett's oesophagus or early oesophageal adenocarcinoma. There will not be extra procedures involved. The experimental part of the procedure, using Polyscope multispectral endoscope will prolong the procedure in most cases by approximately 5-10 minutes

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Barrett Esophagus, Esophageal Neoplasms, Reflux Esophagitis
Keywords
Barrett Esophagus, Endoscopy, Adenocarcinoma

7. Study Design

Primary Purpose
Device Feasibility
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
20 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Barrett's Esophagus patients
Arm Type
Experimental
Arm Description
Multi-Spectral Endoscopic Imaging
Intervention Type
Device
Intervention Name(s)
Endoscopy with Polyscope (Polydiagnost TM) coupled with Multi-Spectral Imaging light-source
Intervention Description
During surveillance endoscopy procedure, the endoscopist will insert the multispectral endoscopy probe through the working channel and use this to inspect the Barrett's oesophagus segment and any visible lesions
Primary Outcome Measure Information:
Title
Level of confidence in delineating the area of interest by multispectral imaging
Description
Level of confidence in delineating the area of interest by the multispectral endoscope in terms of image quality and visibility of area of interest assessed by endoscopist using a 1 to 10 Visual Analogue Score (VAS). We will consider the following ranges 0-3 poor; 4-5 fair; 6-8 good, 9-10 excellent
Time Frame
1 year
Secondary Outcome Measure Information:
Title
Imaging spectra by multispectral endoscopy in neoplastic vs. non-neoplastic Barrett's
Description
Number and type of image spectra corresponding to neoplastic and non-neoplastic area of Barrett's Oesophagus
Time Frame
1 year
Title
Patient comfort
Description
Patient comfort score measured by assisting nurse according to standard scoring scale (1 to 5)
Time Frame
1 year
Title
Time
Description
Time to perform multispectral imaging in minutes
Time Frame
1 year
Title
Correlation with molecular biomarkers
Description
Comparison of the biomarker features of biopsies directed by multispectral imaging (both neoplastic and non-neoplastic) using a molecular panel assessing aneuploidy, p53 and cyclin A.
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Male or female subjects over 18 years Previous diagnosis of Barrett's oesophagus, with an endoscopic length of at least 2 cm Previous diagnosis of oesophageal glandular dysplasia or early oesophageal adenocarcinoma for consideration of endoscopic therapy Exclusion Criteria: History of oesophageal stricture precluding passage of the endoscope, Pregnancy, or planned pregnancy during the course of the study, Currently breastfeeding Any history of esophageal varices, liver impairment of moderate or worse severity (Child's- Pugh class B & C) or evidence of varices on initial treatment endoscopy, Any history of oesophageal surgery, except for uncomplicated fundoplication, and, History of coagulopathy, with INR>1.3 and/or platelet count of <75,000. On clopidogrel, and/or warfarin for high risk condition and unable to withhold temporarily the medication.
Facility Information:
Facility Name
MRC Cancer Unit
City
Cambridge
ZIP/Postal Code
CB2 0XZ
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
No
Citations:
PubMed Identifier
34628734
Citation
Waterhouse DJ, Bano S, Januszewicz W, Stoyanov D, Fitzgerald RC, di Pietro M, Bohndiek SE. First-in-human pilot study of snapshot multispectral endoscopy for early detection of Barrett's-related neoplasia. J Biomed Opt. 2021 Oct;26(10):106002. doi: 10.1117/1.JBO.26.10.106002.
Results Reference
derived

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Feasibility of Multi-Spectral Endoscopic Imaging for Detection of Early Neoplasia in Barrett's Oesophagus

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