UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000044622
Receipt number R000050971
Scientific Title A multicenter study for colorectal polyp detection performance of Computer-Aided-Detection (CADe) system for endoscopy
Date of disclosure of the study information 2021/06/22
Last modified on 2022/07/05 16:14:21

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Basic information

Public title

Performance evaluation of Computer-Aided polyp Detection system with artificial intelligence (AI) for colonoscopy

Acronym

Performance evaluation of Computer-Aided polyp Detection system for colonoscopy

Scientific Title

A multicenter study for colorectal polyp detection performance of Computer-Aided-Detection (CADe) system for endoscopy

Scientific Title:Acronym

Performance evaluation of endoscopy CADe system

Region

Japan


Condition

Condition

Colorectal lesion type 0 in the classification of gross appearance.

Classification by specialty

Hepato-biliary-pancreatic medicine

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the colorectal lesion detection performance of the CADe system for endoscopy.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Sensitivity for detecting the colorectal lesion of the CADe system.

Key secondary outcomes



Base

Study type

Observational


Study design

Basic design


Randomization


Randomization unit


Blinding


Control


Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms


Purpose of intervention


Type of intervention


Interventions/Control_1


Interventions/Control_2


Interventions/Control_3


Interventions/Control_4


Interventions/Control_5


Interventions/Control_6


Interventions/Control_7


Interventions/Control_8


Interventions/Control_9


Interventions/Control_10



Eligibility

Age-lower limit

20 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Patients who undergo total colonoscopy at the institutions during the study period.

Key exclusion criteria

Patients who:
- have been diagnosed with inflammatory bowel disease;
- have been diagnosed with polyposis coli;
- do not agree to participate in this study;
- are under the age of 20;
- undergo colonoscopy as treatment;
- underwent total proctocolectomy in the past;
- are participating in other clinical studies or trials that might have direct or indirect effects on results from this study;
- cannot observe instructions of this study and colonoscopy and;
- are judged to be inappropriate as a subject of this study by the principal investigator, for other reasons.

Target sample size

440


Research contact person

Name of lead principal investigator

1st name Masahiro
Middle name
Last name Igarashi

Organization

Cancer Institute Hospital, Japanese Foundation for Cancer Research

Division name

Digestive of Gastroenterology

Zip code

135-8550

Address

3-8-31 Ariake,Koto-ku, Tokyo, Japan

TEL

03-3520-0111

Email

masahiro.igarashi@jfcr.or.jp


Public contact

Name of contact person

1st name Akiko
Middle name
Last name Chino

Organization

Cancer Institute Hospital, Japanese Foundation for Cancer Research

Division name

Digestive of Gastroenterology

Zip code

135-8550

Address

3-8-31 Ariake,Koto-ku, Tokyo, Japan

TEL

03-3520-0111

Homepage URL


Email

akiko.chino@jfcr.or.jp


Sponsor or person

Institute

Cancer Institute Hospital, Japanese Foundation for Cancer Research

Institute

Department

Personal name



Funding Source

Organization

OLYMPUS Medical Systems Corp.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Cancer Institute Hospital, Japanese Foundation for Cancer Research

Address

3-8-31 Ariake,Koto-ku, Tokyo, Japan, 135-8550

Tel

03-3520-0111

Email

med.shinsa@jfcr.or.jp


Secondary IDs

Secondary IDs

NO

Study ID_1


Org. issuing International ID_1


Study ID_2


Org. issuing International ID_2


IND to MHLW



Institutions

Institutions



Other administrative information

Date of disclosure of the study information

2021 Year 06 Month 22 Day


Related information

URL releasing protocol

N/A

Publication of results

Published


Result

URL related to results and publications

https://www.jddw.jp/jddw2021/abstracts/abst/40590.html

Number of participants that the trial has enrolled

185

Results

In this study, 185 cases were identified for evaluation and 557 lesions were determined by the endoscopists as the gold standard. The results of this study showed that the lesion detection sensitivity of the colonoscopy CADe system was 97.5%.

Results date posted

2022 Year 07 Month 05 Day

Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics

male: 122, female: 63

Participant flow

Of the subjects who met the inclusion criteria and not violate the exclusion criteria, 185 subjects with lesions were included in this study and all were analyzed.

Adverse events

N/A

Outcome measures

The sensitivity evaluated as the primary endpoint was 97.5% [95%CI: 95.8-98.5%].

Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Completed

Date of protocol fixation

2019 Year 08 Month 20 Day

Date of IRB

2019 Year 09 Month 26 Day

Anticipated trial start date

2019 Year 12 Month 19 Day

Last follow-up date

2020 Year 08 Month 15 Day

Date of closure to data entry

2020 Year 08 Month 21 Day

Date trial data considered complete

2021 Year 04 Month 20 Day

Date analysis concluded

2021 Year 05 Month 25 Day


Other

Other related information

A total of four institutes participating in this joint study including the Cancer Institute Hospital of JFCR performed colonoscopy from December 2019 to August 2020. The performance of the CADe system for endoscopy was evaluated with videos, which were recorded during the colonoscopy after obtaining informed consent from the patients.


Management information

Registered date

2021 Year 06 Month 22 Day

Last modified on

2022 Year 07 Month 05 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000050971


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name