UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000044823
Receipt number R000051195
Scientific Title Educational intervention study for establishing a safe learning method with a novel duodenal simulator model
Date of disclosure of the study information 2021/07/10
Last modified on 2023/01/11 06:40:24

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Basic information

Public title

Educational intervention study for establishing a safe learning method with a novel duodenal simulator model

Acronym

Educational intervention study for establishing a safe learning method with a novel duodenal simulator model

Scientific Title

Educational intervention study for establishing a safe learning method with a novel duodenal simulator model

Scientific Title:Acronym

Educational intervention study for establishing a safe learning method with a novel duodenal simulator model

Region

Japan


Condition

Condition

Gastroenterologists and resident doctors performing endoscopic retrograde cholangiopancreatography and endoscopic sphincterotomy

Classification by specialty

Gastroenterology Hepato-biliary-pancreatic medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To clarify the efficacy of hands-on training for trainees with a novel duodenal simulator model

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Comparison of Visual Analog Scale score between before and after simulator training for trainees

Key secondary outcomes

To clarify factors related to complete duodenal papillotomy and lithotripsy: such as number of years of experience, number of cases experienced, and appropriate use of each device in each situation


Base

Study type

Interventional


Study design

Basic design

Single arm

Randomization

Non-randomized

Randomization unit


Blinding

Open -no one is blinded

Control

Uncontrolled

Stratification


Dynamic allocation

NO

Institution consideration


Blocking

NO

Concealment

No need to know


Intervention

No. of arms

1

Purpose of intervention

Educational,Counseling,Training

Type of intervention

Other

Interventions/Control_1

Gastroenterologists and resident doctors performing endoscopic retrograde cholangiopancreatography and endoscopic sphincterotomy

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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Gastroenterologists and resident doctors performing endoscopic retrograde cholangiopancreatography and endoscopic sphincterotomy

Key exclusion criteria

a person cannot consent to the study

Target sample size

30


Research contact person

Name of lead principal investigator

1st name Takeshi
Middle name
Last name Kanno

Organization

Tohoku University Hospital

Division name

Department of Education and Support for Regional Medicine

Zip code

980-8575

Address

1-1 Seiryo-cho, Aoba-ku, Sendai City, Miyagi Prefecture

TEL

022-717-7000

Email

kanno.takeshi@med.tohoku.ac.jp


Public contact

Name of contact person

1st name Yutaka
Middle name
Last name Hatayama

Organization

Tohoku University Hospital

Division name

Department of Gastroenterology

Zip code

980-8575

Address

1-1 Seiryo-cho, Aoba-ku, Sendai City, Miyagi Prefecture

TEL

022-717-7171

Homepage URL


Email

yutaka.hatayama.e4@tohoku.ac.jp


Sponsor or person

Institute

Tohoku University

Institute

Department

Personal name



Funding Source

Organization

Foundation for Promotion of Endoscopic Medical Research

Organization

Division

Category of Funding Organization

Non profit foundation

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Ethics Committee of Tohoku University Hospital

Address

1-1 Seiryo-cho, Aoba-ku, Sendai City, Miyagi Prefecture

Tel

022-717-7000

Email

rinri-esct@proj.med.tohoku.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



Other administrative information

Date of disclosure of the study information

2021 Year 07 Month 10 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

Enrolling by invitation

Date of protocol fixation

2021 Year 03 Month 25 Day

Date of IRB

2021 Year 04 Month 13 Day

Anticipated trial start date

2022 Year 04 Month 18 Day

Last follow-up date

2024 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2021 Year 07 Month 10 Day

Last modified on

2023 Year 01 Month 11 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000051195


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name