UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000054068
Receipt number R000061733
Scientific Title A study on small bowel scrutiny in diarrhoea associated with the administration of immune checkpoint inhibitors.
Date of disclosure of the study information 2024/04/05
Last modified on 2024/04/04 23:36:49

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Basic information

Public title

A study on small bowel scrutiny in diarrhoea associated with the administration of immune checkpoint inhibitors.

Acronym

A study on small bowel scrutiny in diarrhoea associated with the administration of immune checkpoint inhibitors.

Scientific Title

A study on small bowel scrutiny in diarrhoea associated with the administration of immune checkpoint inhibitors.

Scientific Title:Acronym

A study on small bowel scrutiny in diarrhoea associated with the administration of immune checkpoint inhibitors.

Region

Japan


Condition

Condition

Diarrhoea associated with administration of immune checkpoint inhibitors

Classification by specialty

Gastroenterology

Classification by malignancy

Malignancy

Genomic information

YES


Objectives

Narrative objectives1

To investigate mucosal changes in the small intestine in patients with diarrhoea associated with the administration of immune checkpoint inhibitors.

Basic objectives2

Safety

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Prevalence of small bowel capsule endoscopy.

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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1) Patients with suspected diarrhoea associated with ICI administration
2) Patients for whom small bowel capsule endoscopy is (or was) performed for the purpose of ICI scrutiny.
3) Men and women aged 18 years and over at the time of small bowel capsule endoscopy.

Key exclusion criteria

(1) Patients who have refused to participate in response to the opt-out.

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Misawa
Middle name
Last name Noboru

Organization

Yokohama City University Hospital

Division name

Endoscopy centre

Zip code

236-0004

Address

3-9, Fukuura, Kanazawa-ku, Yokohama

TEL

0457872800

Email

nobomisa@hotmail.co.jp


Public contact

Name of contact person

1st name Misawa
Middle name
Last name Noboru

Organization

Yokohama City University Hospital

Division name

Endoscopy centre

Zip code

247-0006

Address

3-9, Fukuura, Kanazawa-ku, Yokohama

TEL

09061961466

Homepage URL


Email

nobomisa@hotmail.co.jp


Sponsor or person

Institute

Yokohama City University

Institute

Department

Personal name



Funding Source

Organization

Yokohama City University

Organization

Division

Category of Funding Organization

Other

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Yokohama City University Hospital

Address

s

Tel

0457872800

Email

nobomisa@hotmail.co.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

2024 Year 04 Month 05 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

Open public recruiting

Date of protocol fixation

2023 Year 07 Month 03 Day

Date of IRB

2022 Year 08 Month 03 Day

Anticipated trial start date

2023 Year 09 Month 01 Day

Last follow-up date

2026 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

None in particular.


Management information

Registered date

2024 Year 04 Month 04 Day

Last modified on

2024 Year 04 Month 04 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000061733


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name