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Optical Polyp Testing for In Vivo Classification (OPTIC)

Primary Purpose

Colonic Polyp, Colonic Diseases, Colonic Neoplasms

Status
Completed
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
Optical spectral reflectance and autofluorescence imaging
Sponsored by
Imperial College London
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional device feasibility trial for Colonic Polyp focused on measuring Endoscopy, Colonoscopy, Hyperspectral imaging, Tissue classification, Tissue autofluorescence, Advanced imaging techniques

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Inclusion Criteria:

  • All patients attending for screening colonoscopy, urgent colonoscopy for altered bowel habit (on a two week wait) or those patients attending for polyp surveillance or therapy.

Exclusion Criteria:

  • Patients with colitis, familial adenomatous polyposis or those that have undergone previous surgery as these different pathologies may confound interpretation of the optical signals.
  • At the discretion of the endoscopist patients with poor bowel preparation will be excluded if it is judged that the colonoscopy cannot be completed. Further quality measures will be determined for reliable data acquisition (see outcome measures).
  • Patients with acute gastrointestinal bleeding
  • Patients with chronic liver disease
  • Patients with abnormal coagulation or any other contra-indication to use of standard biopsy in routine diagnostic endoscopic procedures
  • Patients who are unable or unwilling to give informed consent
  • Patients under the age of 18 years
  • Patients unable to speak English

Sites / Locations

  • Imperial College London

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

Imaging using OPTIC probe

Arm Description

Single arm study to test the feasibility of a new device - the OPTIC imaging probe. All participants enrolled in the study may be imaged using optical spectral reflectance and autofluorescence imaging during their endoscopy procedure.

Outcomes

Primary Outcome Measures

Diagnostic accuracy of hyperplastic vs adenoma classification
Correlation of optical signals from colonic polyps and their histologically-confirmed diagnosis. Quantification of sensitivity, specificity, negative predictive value.

Secondary Outcome Measures

Extension of classification algorithm to other polyp types (higher grade adenomas and cancer)
Sensitivity and specificity of measured optical signals in differentiating different grades of adenoma.
Bowel preparation quality
Is bowel preparation quality sufficient for endoscopy to proceed? Bowel preparation for some patients may be imperfect and hamper collection of optical data. A measure of the quality and hence, reliability, of the measured data must be obtained for future reference in order to prevent erroneous readings.
Mean time added to endoscopy due to additional imaging
An estimate of the time added to an endoscopic examination of the colon due to the need to insert and remove the OPTIC probe

Full Information

First Posted
April 24, 2017
Last Updated
April 12, 2019
Sponsor
Imperial College London
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1. Study Identification

Unique Protocol Identification Number
NCT03139942
Brief Title
Optical Polyp Testing for In Vivo Classification
Acronym
OPTIC
Official Title
Optical Polyp Testing for In Vivo Classification
Study Type
Interventional

2. Study Status

Record Verification Date
April 2019
Overall Recruitment Status
Completed
Study Start Date
March 14, 2017 (Actual)
Primary Completion Date
July 11, 2017 (Actual)
Study Completion Date
July 11, 2017 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Imperial College London

4. Oversight

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

5. Study Description

Brief Summary
Small growths detected in the colon (polyps) during a colonoscopy may or may not have the potential to develop into cancer. However, since visual inspection alone cannot separate all potentially harmful polyps from harmless ones, the standard approach is to remove them all for histological lab examination, exposing patients to risk of injury and putting a significant demand on hospital resources. An accurate method of determining polyp type during endoscopy would enable the clinician to only remove potentially harmful polyps. A new endoscopic optical imaging probe (OPTIC), which analyses how light interacts with tissue, is proposed to do this. The probe is contained within a normal endoscope and uses white light and blue/violet laser light to illuminate the tissue. The reflected and fluorescent light emitted, along with normal colour pictures of the polyp surface, are measured and recorded to quantify specific characteristics of each type. Optical measurements of polyps detected in endoscopy clinics at Imperial College Healthcare NHS Trust will be analysed to determine if the signal can be used to differentiate different polyp types.
Detailed Description
Polyps detected during a colonoscopy may range from benign to precancerous and cancerous. While experienced endoscopists can reliably recognise cancer, the difference between small polyps that have the potential to develop into cancer (adenomas) and those that do not (hyperplastic), is often ambiguous. The standard approach is to simply remove all polyps and analyse them in the histology lab. This means that many patients with hyperplastic polyps (40% of those detected) are unnecessarily exposed to risk of injury (bowel perforation and bleeding) during removal. Furthermore the NHS faces the significant cost of diagnosing this harmless colon tissue. If clinicians were able to accurately determine polyp type during endoscopy, without removal, then hyperplastic tissue could be left alone while potentially harmful tissue is removed. A pilot study of a new endoscopic optical imaging probe (OPTIC), which analyses how different colours of light interact with tissue, is proposed. Previous research has indicated that these properties differ in hyperplastic and adenomatous polyps. The probe is contained within a normal endoscope and uses white light and blue/violet laser light to illuminate the tissue. The reflected and fluorescent light emitted, along with normal colour pictures of the polyp surface, are measured and recorded to quantify specific characteristics of each type. Patients attending endoscopy clinics at Imperial College Healthcare NHS Trust will be asked to allow the use of the OPTIC probe during their colonoscopy. If the clinician detects a polyp that he/she intends to remove then this will be analysed using OPTIC before removal. The histology results from the tissue sample will be recorded and correlated to the OPTIC probe measurements. The resulting library of optical data will be used to design software to automatically categorise unknown polyps based on the OPTIC signal. The accuracy of the technique will be compared to the clinicians' visual assessments. The patients' involvement in the study ceases after the colonoscopy.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colonic Polyp, Colonic Diseases, Colonic Neoplasms, Colonic Adenoma, Colonic Adenocarcinoma, Colonic Dysplasia, Colonic Carcinoma, Colonic Cancer, Colon Hyperplastic Polyp
Keywords
Endoscopy, Colonoscopy, Hyperspectral imaging, Tissue classification, Tissue autofluorescence, Advanced imaging techniques

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
13 (Actual)

8. Arms, Groups, and Interventions

Arm Title
Imaging using OPTIC probe
Arm Type
Experimental
Arm Description
Single arm study to test the feasibility of a new device - the OPTIC imaging probe. All participants enrolled in the study may be imaged using optical spectral reflectance and autofluorescence imaging during their endoscopy procedure.
Intervention Type
Device
Intervention Name(s)
Optical spectral reflectance and autofluorescence imaging
Intervention Description
When a suitable area of tissue is identified by the clinician during a patient's colonoscopy (e.g., a polyp), the imaging probe is inserted into the colonoscope so that it can view the tissue. Optical spectral reflectance and autofluorescence imaging is then performed to collect white light reflected by, and fluorescent light emitted from, the tissue. This is then analysed by hardware and software components in the external analysis unit.
Primary Outcome Measure Information:
Title
Diagnostic accuracy of hyperplastic vs adenoma classification
Description
Correlation of optical signals from colonic polyps and their histologically-confirmed diagnosis. Quantification of sensitivity, specificity, negative predictive value.
Time Frame
1-2 weeks (from day of endoscopy and optical measurement, to return of histology results for any detected polyp)
Secondary Outcome Measure Information:
Title
Extension of classification algorithm to other polyp types (higher grade adenomas and cancer)
Description
Sensitivity and specificity of measured optical signals in differentiating different grades of adenoma.
Time Frame
1-2 weeks (from day of endoscopy and optical measurement, to return of histology results for any detected polyp)
Title
Bowel preparation quality
Description
Is bowel preparation quality sufficient for endoscopy to proceed? Bowel preparation for some patients may be imperfect and hamper collection of optical data. A measure of the quality and hence, reliability, of the measured data must be obtained for future reference in order to prevent erroneous readings.
Time Frame
1 day (has bowel preparation been sufficient on day of endoscopy and optical measurement)
Title
Mean time added to endoscopy due to additional imaging
Description
An estimate of the time added to an endoscopic examination of the colon due to the need to insert and remove the OPTIC probe
Time Frame
1 day

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Inclusion Criteria: All patients attending for screening colonoscopy, urgent colonoscopy for altered bowel habit (on a two week wait) or those patients attending for polyp surveillance or therapy. Exclusion Criteria: Patients with colitis, familial adenomatous polyposis or those that have undergone previous surgery as these different pathologies may confound interpretation of the optical signals. At the discretion of the endoscopist patients with poor bowel preparation will be excluded if it is judged that the colonoscopy cannot be completed. Further quality measures will be determined for reliable data acquisition (see outcome measures). Patients with acute gastrointestinal bleeding Patients with chronic liver disease Patients with abnormal coagulation or any other contra-indication to use of standard biopsy in routine diagnostic endoscopic procedures Patients who are unable or unwilling to give informed consent Patients under the age of 18 years Patients unable to speak English
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Julian P Teare, MD FRCP
Organizational Affiliation
Imperial College London
Official's Role
Principal Investigator
Facility Information:
Facility Name
Imperial College London
City
London
ZIP/Postal Code
SW7 2AZ
Country
United Kingdom

12. IPD Sharing Statement

Plan to Share IPD
Undecided
IPD Sharing Plan Description
Only anonymised data will be shared. The research team may share findings from the study with non-Imperial College academic collaborators, who will further develop aspects of its imaging capabilities.

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Optical Polyp Testing for In Vivo Classification

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