UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000053424
Receipt number R000060961
Scientific Title Comparison of gastric lesion detection performance between a CADe program for endoscopy and doctors
Date of disclosure of the study information 2024/01/31
Last modified on 2024/01/24 11:51:07

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Basic information

Public title

Performance evaluation of a computer-aided gastric lesion detection program: comparison with doctors

Acronym

Performance evaluation of a computer-aided-detection (CADe) program

Scientific Title

Comparison of gastric lesion detection performance between a CADe program for endoscopy and doctors

Scientific Title:Acronym

Performance evaluation of a CADe program: comparison with doctors

Region

Japan


Condition

Condition

Localized gastric lesions

Classification by specialty

Gastroenterology

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

To evaluate the gastric lesion detection performance of a CADe program for endoscopy

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Comparison of sensitivity between the CADe program for endoscopy and doctors

Key secondary outcomes

Comparison of specificity between the CADe program for endoscopy and doctors


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 with early-stage gastric cancer who have undergone upper gastrointestinal endoscopy

Key exclusion criteria

Patients who:
- underwent total gastrectomy;
- are under the age of 20;
- do not agree to participate in this study and;
- are judged to be inappropriate as a subject of this study by the investigator, for other reasons.

Target sample size

317


Research contact person

Name of lead principal investigator

1st name Kenshi
Middle name
Last name Yao

Organization

Fukuoka University Chikushi Hospital

Division name

Department of Endoscopy

Zip code

818-8502

Address

1-1-1 Zokumyoin, Chikushino-shi, Fukuoka

TEL

092-921-1011

Email

yao@fukuoka-u.ac.jp


Public contact

Name of contact person

1st name Kenshi
Middle name
Last name Yao

Organization

Fukuoka University Chikushi Hospital

Division name

Department of Endoscopy

Zip code

818-8502

Address

1-1-1 Zokumyoin, Chikushino-shi, Fukuoka

TEL

092-921-1011

Homepage URL


Email

yao@fukuoka-u.ac.jp


Sponsor or person

Institute

Fukuoka Uninersity Chikushi Hospital

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

Fukuoka University Chikushi Hospital

Address

1-1-1 Zokumyoin, Chikushino-shi, Fukuoka

Tel

092-921-1011

Email

chikushirinsho@adm.fukuoka-u.ac.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

静岡がんセンター(静岡県)、千葉大学医学部附属病院(千葉県)、
神戸市立医療センター中央市民病院(兵庫県)、
オリンパスメディカルシステムズ株式会社(東京都)


Other administrative information

Date of disclosure of the study information

2024 Year 01 Month 31 Day


Related information

URL releasing protocol


Publication of results

Unpublished


Result

URL related to results and publications


Number of participants that the trial has enrolled


Results


Results date posted


Results Delayed


Results Delay Reason


Date of the first journal publication of results


Baseline Characteristics


Participant flow


Adverse events


Outcome measures


Plan to share IPD


IPD sharing Plan description



Progress

Recruitment status

Preinitiation

Date of protocol fixation

2023 Year 10 Month 20 Day

Date of IRB

2023 Year 11 Month 01 Day

Anticipated trial start date

2024 Year 04 Month 01 Day

Last follow-up date

2024 Year 09 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Endoscopy videos and data in retrospectively collected cases meeting the inclusion criteria were used to compare sensitivity between the CADe program for endoscopy and doctors.


Management information

Registered date

2024 Year 01 Month 24 Day

Last modified on

2024 Year 01 Month 24 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000060961


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name