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Development and Validation of a Deep Learning Algorithm to Evaluate Endoscopic Disease Activity of Ulcerative Colitis.

Primary Purpose

Ulcerative Colitis

Status
Unknown status
Phase
Not Applicable
Locations
China
Study Type
Interventional
Intervention
Artificial inteligence associated ulcerative colitis severity scoring system
Conventional human scoring
Sponsored by
Shandong University
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional health services research trial for Ulcerative Colitis focused on measuring Ulcerative Colitis, Deep Learning, Convolutional Neural Network

Eligibility Criteria

18 Years - 70 Years (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patients with ulcerative colitis undergoing colonoscopy

Exclusion Criteria:

  • Known or suspected bowel obstruction, stricture or perforation
  • Compromised swallowing reflex or mental status
  • Severe congestive heart failure (New York Heart Association class III or IV)
  • Uncontrolled hypertension (systolic blood pressure > 170 mm Hg, diastolic blood pressure > 100 mm Hg)
  • Pregnancy or lactation
  • Hemodynamically unstable
  • Colonic surgery history
  • Bad bowel preparation (segmental BBPS<2)
  • Unable to give informed consent

Sites / Locations

  • Qilu hosipital

Arms of the Study

Arm 1

Arm 2

Arm Type

Experimental

Active Comparator

Arm Label

Artificial Intelligence assisted Scoring Group

Conventional Human Scoring Group

Arm Description

Patients in this group go through colonoscopy under the AI monitoring device.

Patients in this group go through conventional colonoscopy without AI monitoring device.

Outcomes

Primary Outcome Measures

The scoring accuracy of Mayo ES in AI-associated group and conventional group.
The scoring accuracy of Mayo endoscopic sub-score (Mayo ES) in each group will be calculated using scores from expert group as reference standard. The Mayo ES is a 4-point scale, which classifies the endoscopic severity of ulcerative colitis into the following four categories: point 0 refers to normal or inactive disease, point 1 refers to mild disease with erythema, decreased vascular patterns and mild friability, point 2 refers to moderate disease with marked erythema, absence of vascular patterns, friability and erosions, point 3 refers to severe disease with spontaneous bleed and ulceration. The scoring accuracy of Mayo ES ranging from 0 to 3 point will be separately evaluated in both groups.
The scoring accuracy of UCEIS in AI-associated group and conventional group.
The scoring accuracy of Ulcerative colitis endoscopic index of severity (UCEIS) in each group will be separately calculated using scores from expert group as reference standard. The UCEIS is an 8-point scale consists of 3 parts: vascular pattern (point 0 refers to normal mucosa, point 1 refers to patchy obliteration of vascular pattern, point 2 refers to complete obliteration of vascular pattern), bleeding (point 0 refers to no visible blood, point 1 refers to some spots of coagulated blood, point 2 refers to free liquid, point 3 refers to frank blood in the lumen), erosions and ulcers (point 0 refers to normal mucosa, point 1 refers to erosions, point 2 refers to superficial ulcers, point 3 refers to deep ulcers. The total UCEIS score summarized by the above 3 parts will be analyzed. The scoring accuracy of UCEIS ranging from 0 to 8 point will be separately evaluated in both group.

Secondary Outcome Measures

The accuracy of mucosal healing judgements using Mayo ES in each group.
The accuracy of mucosal healing judgements using Mayo ES will be calculated in each group. Assessments from expert group will be used as reference standard. Complete mucosal healing is defined as point 0 in Mayo ES scale, which refers to normal or inactive disease.
The accuracy of mucosal healing judgements using UCEIS in each group.
The accuracy of mucosal healing judgements using UCEIS will also be calculated in each group. Assessments from expert group will be used as reference standard. Complete mucosal healing is defined as point 0 in UCEIS scale, which refers to normal vascular pattern without bleeding, erosions and ulceration.

Full Information

First Posted
May 27, 2019
Last Updated
June 1, 2019
Sponsor
Shandong University
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1. Study Identification

Unique Protocol Identification Number
NCT03973437
Brief Title
Development and Validation of a Deep Learning Algorithm to Evaluate Endoscopic Disease Activity of Ulcerative Colitis.
Official Title
Real-time Evaluation of Severity and Mucosal Healing in Patients With Ulcerative Colitis by a Deep Learning Algorithm: a Multi-center Prospective Study.
Study Type
Interventional

2. Study Status

Record Verification Date
June 2019
Overall Recruitment Status
Unknown status
Study Start Date
June 1, 2019 (Anticipated)
Primary Completion Date
December 31, 2019 (Anticipated)
Study Completion Date
June 1, 2020 (Anticipated)

3. Sponsor/Collaborators

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

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
The purpose of this study is to develop an artificial intelligence(AI) assisted scoring system, which can evaluate the disease severity and mucosal healing stage in patients with ulcerative colitis. Then testify whether this new scoring system can help physicians to enhance the accuracy of disease severity assessments in a multi-center clinical practice.
Detailed Description
Ulcerative colitis is a non-specific chronic inflammation of gut characterized by referral bloody stool, diarrhea and abdominal pain. Endoscopic features of the disease severity and mucosal healing stage are strongly associated with treatment response and prognosis in the future. Currently, the Mayo endoscopic sub-score (Mayo ES) and Ulcerative colitis endoscopic index of severity (UCEIS) are commonly recommended to guide therapeutic adjustments. However, the accuracy of these scales greatly relies on intra-observer and inter-observer consistency for lack of objective measurements. Recently, deep learning algorithm based on convolutional neural network (CNN) has shown multiple potential in computer-aided detection and computer-aided diagnose of gastrointestinal lesions. Up to now, no randomized controlled trials have been conducted to evaluate the performance of deep learning algorithm for assessing disease activity in ulcerative colitis. This study aims to train a deep learnig algorithm to assess severity and mucosal healing stage of ulcerative colitis using the Mayo ES and UCEIS scale, then testify whether the engagement of AI can improve the evaluation accuracy of physicians in a multi-center clinical practice.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Ulcerative Colitis
Keywords
Ulcerative Colitis, Deep Learning, Convolutional Neural Network

7. Study Design

Primary Purpose
Health Services Research
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
Outcomes Assessor
Allocation
Randomized
Enrollment
200 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Artificial Intelligence assisted Scoring Group
Arm Type
Experimental
Arm Description
Patients in this group go through colonoscopy under the AI monitoring device.
Arm Title
Conventional Human Scoring Group
Arm Type
Active Comparator
Arm Description
Patients in this group go through conventional colonoscopy without AI monitoring device.
Intervention Type
Device
Intervention Name(s)
Artificial inteligence associated ulcerative colitis severity scoring system
Intervention Description
Patients in this group go through a flexible colonoscopy under the AI monitoring device. During the withdrawal process, inflammatory lesions are detected by AI-associated scoring system. Pictures are automatically captured and analyzed by the computer. The Mayo ES and UCEIS sores will be calculated and presented on a second screen, providing a reference for the physician to evaluate the disease severity and mucosal healing stage of the patient. Biopsies will be taken from inflammatory region for histological examination. Videos will be recorded and re-evaluated by a group of experts to determine the final Mayo ES and UCEIS scores.
Intervention Type
Device
Intervention Name(s)
Conventional human scoring
Intervention Description
Patients in this group go through a conventional colonoscopy without the AI monitoring device. During the withdrawal process, physician evaluates the disease severity and mucosal healing stage of the patient according to his personal experience. Biopsies will be taken from inflammatory region for histological examination. Videos will be recorded and re-evaluated by a group of experts to determine the final Mayo ES and UCEIS scores.
Primary Outcome Measure Information:
Title
The scoring accuracy of Mayo ES in AI-associated group and conventional group.
Description
The scoring accuracy of Mayo endoscopic sub-score (Mayo ES) in each group will be calculated using scores from expert group as reference standard. The Mayo ES is a 4-point scale, which classifies the endoscopic severity of ulcerative colitis into the following four categories: point 0 refers to normal or inactive disease, point 1 refers to mild disease with erythema, decreased vascular patterns and mild friability, point 2 refers to moderate disease with marked erythema, absence of vascular patterns, friability and erosions, point 3 refers to severe disease with spontaneous bleed and ulceration. The scoring accuracy of Mayo ES ranging from 0 to 3 point will be separately evaluated in both groups.
Time Frame
6 months
Title
The scoring accuracy of UCEIS in AI-associated group and conventional group.
Description
The scoring accuracy of Ulcerative colitis endoscopic index of severity (UCEIS) in each group will be separately calculated using scores from expert group as reference standard. The UCEIS is an 8-point scale consists of 3 parts: vascular pattern (point 0 refers to normal mucosa, point 1 refers to patchy obliteration of vascular pattern, point 2 refers to complete obliteration of vascular pattern), bleeding (point 0 refers to no visible blood, point 1 refers to some spots of coagulated blood, point 2 refers to free liquid, point 3 refers to frank blood in the lumen), erosions and ulcers (point 0 refers to normal mucosa, point 1 refers to erosions, point 2 refers to superficial ulcers, point 3 refers to deep ulcers. The total UCEIS score summarized by the above 3 parts will be analyzed. The scoring accuracy of UCEIS ranging from 0 to 8 point will be separately evaluated in both group.
Time Frame
6 months
Secondary Outcome Measure Information:
Title
The accuracy of mucosal healing judgements using Mayo ES in each group.
Description
The accuracy of mucosal healing judgements using Mayo ES will be calculated in each group. Assessments from expert group will be used as reference standard. Complete mucosal healing is defined as point 0 in Mayo ES scale, which refers to normal or inactive disease.
Time Frame
6 months
Title
The accuracy of mucosal healing judgements using UCEIS in each group.
Description
The accuracy of mucosal healing judgements using UCEIS will also be calculated in each group. Assessments from expert group will be used as reference standard. Complete mucosal healing is defined as point 0 in UCEIS scale, which refers to normal vascular pattern without bleeding, erosions and ulceration.
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Maximum Age & Unit of Time
70 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patients with ulcerative colitis undergoing colonoscopy Exclusion Criteria: Known or suspected bowel obstruction, stricture or perforation Compromised swallowing reflex or mental status Severe congestive heart failure (New York Heart Association class III or IV) Uncontrolled hypertension (systolic blood pressure > 170 mm Hg, diastolic blood pressure > 100 mm Hg) Pregnancy or lactation Hemodynamically unstable Colonic surgery history Bad bowel preparation (segmental BBPS<2) Unable to give informed consent
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Xiuli Zuo, MD,PhD
Phone
15588818685
Email
zuoxiuli@sina.com
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Xiuli Zuo, MD,PhD
Organizational Affiliation
Qilu Hospital of Shandong University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Qilu hosipital
City
Jinan
State/Province
Shandong
ZIP/Postal Code
257000
Country
China

12. IPD Sharing Statement

Plan to Share IPD
Yes

Learn more about this trial

Development and Validation of a Deep Learning Algorithm to Evaluate Endoscopic Disease Activity of Ulcerative Colitis.

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