UMIN-ICDS Clinical Trial

Unique ID issued by UMIN UMIN000049465
Receipt number R000056321
Scientific Title Prospective evaluation study of diagnostic ability for biliary disease using novel cholangioscope
Date of disclosure of the study information 2023/01/07
Last modified on 2022/11/09 08:17:50

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Basic information

Public title

Prospective evaluation study of diagnostic ability for biliary disease using novel cholangioscope

Acronym

Prospective evaluation study of diagnostic ability for biliary disease using novel cholangioscope

Scientific Title

Prospective evaluation study of diagnostic ability for biliary disease using novel cholangioscope

Scientific Title:Acronym

Prospective evaluation study of diagnostic ability for biliary disease using novel cholangioscope

Region

Japan


Condition

Condition

Biliary disease

Classification by specialty

Hepato-biliary-pancreatic medicine

Classification by malignancy

Malignancy

Genomic information

NO


Objectives

Narrative objectives1

Diagnostic ability of forceps biopsy for biliary disease under novel cholangioscope

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Diagnostic ability of forceps biopsy for biliary disease under novel cholangioscope

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Historical

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Diagnosis

Type of intervention

Medicine

Interventions/Control_1

Cholangioscope (DRES)

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

Patient with biliary disease who are required for biopsy under cholangioscope. Age >18. IC is obtained.

Key exclusion criteria

Pregnancy, easy bleeding.
Rejection for attending study

Target sample size

50


Research contact person

Name of lead principal investigator

1st name Takeshi
Middle name
Last name Ogura

Organization

Osaka Medical and Pharmaceutical University

Division name

Endoscopy Center

Zip code

5698686

Address

2-7 Daigakuchou, Takatsukishi, Osaka

TEL

072-683-1221

Email

oguratakeshi0411@yahoo.co.jp


Public contact

Name of contact person

1st name Takeshi
Middle name
Last name Ogura

Organization

Osaka Medical and Pharmaceutical University

Division name

Endoscopy Center

Zip code

5698686

Address

2-7 Daigakuchou, Takatsukishi, Osaka

TEL

072-683-1221

Homepage URL


Email

oguratakeshi0411@yahoo.co.jp


Sponsor or person

Institute

Osaka Medical and Pharmaceutical University

Institute

Department

Personal name



Funding Source

Organization

Osaka Medical and Pharmaceutical University

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Osaka Medical and Pharmaceutical University

Address

2-7 Daigakuchou, Takatsukishi, Osaka

Tel

072-683-1221

Email

oguratakeshi0411@yahoo.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

2023 Year 01 Month 07 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

2022 Year 09 Month 19 Day

Date of IRB


Anticipated trial start date

2023 Year 01 Month 07 Day

Last follow-up date

2027 Year 07 Month 01 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2022 Year 11 Month 09 Day

Last modified on

2022 Year 11 Month 09 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/icdr_e/ctr_view.cgi?recptno=R000056321


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name