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Clinical Validation of PolyDeep: an Artificial Intelligence-based Computer-aided Polyp Detection (CADe) and Characterization (CADx) System. Polydeep Advance 3

Primary Purpose

Colorectal Cancer

Status
Not yet recruiting
Phase
Not Applicable
Locations
Spain
Study Type
Interventional
Intervention
High definition colonoscopy (standard colonoscopy) in Adenoma Detection Rate
PolyDeep assisted high definition colonoscopy (CAD system) in Adenoma Detection Rate
Sponsored by
Fundacin Biomedica Galicia Sur
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional diagnostic trial for Colorectal Cancer focused on measuring Colorectal adenomas, Colorectal polyps, Serrated lesions, Polydeep, computer-aided System

Eligibility Criteria

40 Years - 79 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • First diagnostic colonoscopy performed after a positive fecal immunochemical test performed within the CRC screening program.
  • Surveillance after resection of colorectal adenomas
  • Acceptance after reading the information sheet and signing informed consent.

Exclusion Criteria:

  • Colonoscopies with insufficient intestinal cleansing (Boston Bowel Preparation Scale <6 or <2 in any of the evaluated segments).
  • Incomplete colonoscopy without cecal intubation.
  • Previous CRC
  • Previous colonic resection.
  • Hereditary CRC syndromes
  • Serrated polyposis syndrome

Sites / Locations

  • Hospital Álvaro Cunqueiro (Vigo)
  • Complexo Hospitalario Universitario de Ourense
  • Hospital de Montecelo

Arms of the Study

Arm 1

Arm 2

Arm Type

Other

Experimental

Arm Label

Control arm: High definition colonoscopy

PolyDeep assisted high definition colonoscopy

Arm Description

Diagnostic test: Standard colonoscopy

Diagnostic test: PolyDeep

Outcomes

Primary Outcome Measures

Adenoma Detection Rate (ADR)
Number of colonoscopies with adenomas/total number of colonoscopies. The investigators will evaluate if there are differences between both arms.

Secondary Outcome Measures

Polyp detection rate
Number of colonoscopies with polyps/total number of colonoscopies. The investigators will evaluate if there are differences between both arms.
Serrated lesion detection rate
Number of colonoscopies with serrated lesions/total number of colonoscopies. The investigators will evaluate if there are differences between both arms.
Advanced lesion detection rate
Number of colonoscopies with advanced lesions (adenomas≥10mm, villous histology or high grade dysplasia; serrated lesions with dysplasia or ≥10mm) /total number of colonoscopies. The investigators will evaluate if there are differences between both arms.
Withdrawal time:
Withdrawal time between the two arms will be calculated and compared by the investigators
Characterization of the detected lesions.
The investigators will evaluate the optical diagnosis accuracy of Polydeep for the final histological diagnosis (sensitivity, specificity, positive and negative predictive values).

Full Information

First Posted
August 22, 2022
Last Updated
April 17, 2023
Sponsor
Fundacin Biomedica Galicia Sur
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1. Study Identification

Unique Protocol Identification Number
NCT05513261
Brief Title
Clinical Validation of PolyDeep: an Artificial Intelligence-based Computer-aided Polyp Detection (CADe) and Characterization (CADx) System. Polydeep Advance 3
Official Title
PolyDeep Advance 3: Randomized Clinical Trial Comparing High Definition Colonoscopy With PolyDeep Assisted High Definition Colonoscopy.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2022
Overall Recruitment Status
Not yet recruiting
Study Start Date
July 2, 2023 (Anticipated)
Primary Completion Date
November 1, 2023 (Anticipated)
Study Completion Date
December 31, 2023 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Fundacin Biomedica Galicia Sur

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
This study is a clinical validation of PolyDeep, a computer-aided polyp detection (CADe) and characterization (CADx) system. PolyDeep Advance 3 is a multicentric randomized clinical trial comparing high definition colonoscopy with PolyDeep assisted high definition colonoscopy. The hypothesis of the study is that the PolyDeep assisted colonoscopy increases the Adenoma Detection Rate (ADR).
Detailed Description
Colorectal cancer (CRC) is the most frequently cancer in western world. A fundamental tool for detection and prevention is the colonoscopy. The detection and endoscopic resection of colorectal polyps, the precursor lesion of CRC, can reduce CRC incidence and mortality. Adenoma Detection Rate is the most used endoscopic quality indicator. The improvement of this indicator is related to the reduction of postcolonoscopy CRC incidence and mortality. Colorectal polyp diagnosis is based on endoscopic resection and histological analysis. An accurate optical diagnosis could avoid histological lesion of smaller lesions, reducing the costs associated with histological diagnosis. The NICE (NBI International Colorectal Endoscopic) Classification has proposed use high definition endoscopes that have Narrow Band Imaging (NBI). However, NICE must be used by endoscopists who are sufficiently prepared and who have overcome the learning curve. Therefore, optical histology diagnosis with high accuracy independently of the center and the endoscopist is necessary. Computer Aid Diagnosis (CAD) systems based on Artificial Intelligence are experiencing exponential development in the field of medical image analysis. The development of the CAD system is based on the creation of large databases of endoscopic images and/or videos, on the training, development and validation of diagnostic algorithms in such databases and, finally, on prospective clinical validation in patients undergoing colonoscopy. The goal of CAD systems in colonoscopy is double. First, the CAD system aims to increase the detection of polyps (CADe) in general, and of adenomas and serrated lesions in particular. The second objective is to characterize (CADx) the histology of detected lesion. PolyDeep CAD is a functional prototype. This CAD system is capable of detecting, locating and classifying colorectal polyps. In vivo validation data shows that PolyDeep has high diagnostic accuracy for polyp identification and that this accuracy can be accommodated. The aim of PolyDeep advance 3 is to compare Adenoma Detection Rate differences in a randomized clinical trial. The investigators will compare the Adenoma Detection Rate between high definition colonoscopy and PolyDeep assisted high definition colonoscopy, both in CRC screening and surveillance.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Colorectal Cancer
Keywords
Colorectal adenomas, Colorectal polyps, Serrated lesions, Polydeep, computer-aided System

7. Study Design

Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Model Description
Patients who fulfill criteria will be randomly allocated to high definition colonoscopy or Polydeep assisted high definition colonoscopy.
Masking
None (Open Label)
Allocation
Randomized
Enrollment
854 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Control arm: High definition colonoscopy
Arm Type
Other
Arm Description
Diagnostic test: Standard colonoscopy
Arm Title
PolyDeep assisted high definition colonoscopy
Arm Type
Experimental
Arm Description
Diagnostic test: PolyDeep
Intervention Type
Diagnostic Test
Intervention Name(s)
High definition colonoscopy (standard colonoscopy) in Adenoma Detection Rate
Intervention Description
In the intervention of this arm the investigators will apply the standard colonoscopy without computer-aided colonoscopy (polyDeep)
Intervention Type
Diagnostic Test
Intervention Name(s)
PolyDeep assisted high definition colonoscopy (CAD system) in Adenoma Detection Rate
Intervention Description
In the intervention of this arm the investigators will apply polyDeep assisted high definition colonoscopy (CAD system).
Primary Outcome Measure Information:
Title
Adenoma Detection Rate (ADR)
Description
Number of colonoscopies with adenomas/total number of colonoscopies. The investigators will evaluate if there are differences between both arms.
Time Frame
1.5 years
Secondary Outcome Measure Information:
Title
Polyp detection rate
Description
Number of colonoscopies with polyps/total number of colonoscopies. The investigators will evaluate if there are differences between both arms.
Time Frame
1.5 years
Title
Serrated lesion detection rate
Description
Number of colonoscopies with serrated lesions/total number of colonoscopies. The investigators will evaluate if there are differences between both arms.
Time Frame
1.5 years
Title
Advanced lesion detection rate
Description
Number of colonoscopies with advanced lesions (adenomas≥10mm, villous histology or high grade dysplasia; serrated lesions with dysplasia or ≥10mm) /total number of colonoscopies. The investigators will evaluate if there are differences between both arms.
Time Frame
1.5 years
Title
Withdrawal time:
Description
Withdrawal time between the two arms will be calculated and compared by the investigators
Time Frame
1.5 years
Title
Characterization of the detected lesions.
Description
The investigators will evaluate the optical diagnosis accuracy of Polydeep for the final histological diagnosis (sensitivity, specificity, positive and negative predictive values).
Time Frame
1.5 years

10. Eligibility

Sex
All
Minimum Age & Unit of Time
40 Years
Maximum Age & Unit of Time
79 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: First diagnostic colonoscopy performed after a positive fecal immunochemical test performed within the CRC screening program. Surveillance after resection of colorectal adenomas Acceptance after reading the information sheet and signing informed consent. Exclusion Criteria: Colonoscopies with insufficient intestinal cleansing (Boston Bowel Preparation Scale <6 or <2 in any of the evaluated segments). Incomplete colonoscopy without cecal intubation. Previous CRC Previous colonic resection. Hereditary CRC syndromes Serrated polyposis syndrome
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Joaquín Cubiella Fernandez, MD PhD
Phone
0034988385824
Email
joaquin.cubiella.fernandez@sergas.es
First Name & Middle Initial & Last Name or Official Title & Degree
Miguel Reboiro Jato, PhD
Facility Information:
Facility Name
Hospital Álvaro Cunqueiro (Vigo)
City
Vigo
State/Province
Pontevedra
Country
Spain
Facility Name
Complexo Hospitalario Universitario de Ourense
City
Ourense
ZIP/Postal Code
32003.
Country
Spain
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Joaquín Cubiella, MD, PhD
First Name & Middle Initial & Last Name & Degree
Pedro Davila, Masters degree
Facility Name
Hospital de Montecelo
City
Pontevedra
Country
Spain

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There are not a plan to make Individual Participant Data (IPD)
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Links:
URL
http://polydeep.org/
Description
Polydeep website
URL
https://intranet.pacifico-meetings.com/amsysweb/faces/publicacionOnlineDOI.xhtml?id=711&idComunicacion=160479
Description
43th congress of digestive endoscopy spanish society
URL
https://linkinghub.elsevier.com/retrieve/pii/S246812531930411X
Description
Effect of a deep-learning computer-aided detection system on adenoma detection during colonoscopy (CADe-DB trial): a double-blind randomised study.

Learn more about this trial

Clinical Validation of PolyDeep: an Artificial Intelligence-based Computer-aided Polyp Detection (CADe) and Characterization (CADx) System. Polydeep Advance 3

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