UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000039817
Receipt number R000045405
Scientific Title Study on gender preference of practicing physicians in upper esophagogastroduodenoscopy
Date of disclosure of the study information 2020/03/16
Last modified on 2020/05/19 09:01:24

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Basic information

Public title

Study on gender preference of practicing physicians in upper esophagogastroduodenoscopy

Acronym

Study on gender preference of practicing physicians in upper esophagogastroduodenoscopy

Scientific Title

Study on gender preference of practicing physicians in upper esophagogastroduodenoscopy

Scientific Title:Acronym

Study on gender preference of practicing physicians in upper esophagogastroduodenoscopy

Region

Japan


Condition

Condition

Patients scheduled for esophagogastroduodenoscopy at our hospital

Classification by specialty

Gastroenterology Hepato-biliary-pancreatic medicine

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

We determine the proportion of patients who want a same-sex endoscopist on esophagogastroduodenoscopy.

Basic objectives2

Others

Basic objectives -Others

We identify factors that influence the wish of a same-sex endoscopist.

Trial characteristics_1

Others

Trial characteristics_2

Others

Developmental phase



Assessment

Primary outcomes

Gender preference of subject's administering endoscopist

Key secondary outcomes

Reasons for gender preference


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

1) Patients who needed a esophagogastroduodenoscopy screening test
2) Over 20 years old
3) After the informed consent is sufficient for participation in this study, the study subject's own approval has been obtained.

Key exclusion criteria

1) Patients who cannot communicate.
2) Patients who cannot fill out the questionnaire themselves.

Target sample size

40


Research contact person

Name of lead principal investigator

1st name Sho
Middle name
Last name Suzuki

Organization

Nihon University Hospital

Division name

Division of Gastroenterology and Hepatology, Department of Medicine

Zip code

101-8309

Address

1-6 Kanda Surugadai, Chiyoda-ku, Tokyo

TEL

0332931711

Email

s.sho.salubriter.mail@gmail.com


Public contact

Name of contact person

1st name Kanako
Middle name
Last name Ogura

Organization

Nihon University Hospital

Division name

Division of Gastroenterology and Hepatology, Department of Medicine

Zip code

101-8309

Address

1-6 Kanda Surugadai, Chiyoda-ku, Tokyo

TEL

0332931711

Homepage URL


Email

kogura0809@yahoo.co.jp


Sponsor or person

Institute

Nihon University Hospital

Institute

Department

Personal name



Funding Source

Organization

None

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

Nihon University Hospital Clinical Research Review Committee

Address

1-6 Kanda Surugadai, Chiyoda-ku, Tokyo

Tel

0332931711

Email

kogura0809@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

2020 Year 03 Month 16 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

No longer recruiting

Date of protocol fixation

2020 Year 02 Month 13 Day

Date of IRB

2020 Year 02 Month 13 Day

Anticipated trial start date

2020 Year 03 Month 16 Day

Last follow-up date

2020 Year 10 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

A questionnaire is distributed to the target patients, and the collected responses are analyzed using a chi-square test.


Management information

Registered date

2020 Year 03 Month 14 Day

Last modified on

2020 Year 05 Month 19 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000045405


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name