UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000039819 |
|---|---|
| Receipt number | R000045406 |
| Scientific Title | A study on the gender preference of practitioners in abdominal ultrasonography |
| Date of disclosure of the study information | 2020/03/16 |
| Last modified on | 2020/05/19 09:01:44 |
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Basic information
Public title
A study on the gender preference of practitioners in abdominal ultrasonography
Acronym
A study on the gender preference of practitioners in abdominal ultrasonography
Scientific Title
A study on the gender preference of practitioners in abdominal ultrasonography
Scientific Title:Acronym
A study on the gender preference of practitioners in abdominal ultrasonography
Region
| Japan |
Condition
Condition
Patients scheduled for Abdominal ultrasonography at our hospital
Classification by specialty
| Gastroenterology | Hepato-biliary-pancreatic medicine |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
On abdominal ultrasonography, we determine the proportion of patients who want the same sex.
Basic objectives2
Others
Basic objectives -Others
We identify the factors that influence the desire for same-sex enforcers.
Trial characteristics_1
Others
Trial characteristics_2
Others
Developmental phase
Assessment
Primary outcomes
Gender preference of subject's enforcer
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 abdominal ultrasonography 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
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
k.ogura0809@gmail.com
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
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=R000045406
