UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000053783
Receipt number R000061379
Scientific Title Continuation rates and physicians' perceptions on tinea pedis management in Japan: a web-based survey and prescription analysis
Date of disclosure of the study information 2024/03/05
Last modified on 2024/03/05 15:02:05

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Basic information

Public title

Continuation rates and physicians' perceptions on tinea pedis management in Japan: a web-based survey and prescription analysis

Acronym

Continuation rates and physicians' perceptions on tinea pedis management in Japan: a web-based survey and prescription analysis

Scientific Title

Continuation rates and physicians' perceptions on tinea pedis management in Japan: a web-based survey and prescription analysis

Scientific Title:Acronym

Continuation rates and physicians' perceptions on tinea pedis management in Japan: a web-based survey and prescription analysis

Region

Japan


Condition

Condition

Tinea pedis

Classification by specialty

Dermatology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To understand the reality of prescription continuation for tinea pedis and physicians' perceptions regarding their drug selection for tinea pedis

Basic objectives2

Others

Basic objectives -Others

Not applicable

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

The reality of prescription continuation for tinea pedis and physicians' perceptions and intentions regarding their drug selection for tinea pedis

Key secondary outcomes

Not applicable


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


Not applicable

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

1. Dermatologists who practice tinea pedis treatment

Key exclusion criteria

[Physician Survey] Physicians who do not meet the inclusion criteria

Target sample size

200


Research contact person

Name of lead principal investigator

1st name YUICHIRO
Middle name
Last name TSUNEMI

Organization

Saitama Medical University

Division name

Dermatology

Zip code

350-0495

Address

38 Morohongo, Moroyamamachi, Irumagun, Saitama 350-0495 Japan

TEL

049-276-1111

Email

ytsun-tky@umin.ac.jp


Public contact

Name of contact person

1st name ETSUKO
Middle name
Last name IWASHITA

Organization

QLife Inc.

Division name

Patient Recruitment Dept

Zip code

105-0001

Address

Toranomon 33 Mori-Bld.10F 3-8-21, Toranomon, Minato-Ku, Tokyo 105-0001 Japan

TEL

03-6860-5020

Homepage URL


Email

e-iwashita@qlife.co.jp


Sponsor or person

Institute

Other

Institute

Department

Personal name



Funding Source

Organization

Sato Pharmaceutical Co.,Ltd

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor

Not applicable

Name of secondary funder(s)



IRB Contact (For public release)

Organization

The Ethics Committee of Noguchi Dermatology Clinic

Address

964-1, Uejima, Kashima-machi, Kamimashiki-gun, Kumamoto, 861-3106 Japan

Tel

096-237-4112

Email

derma@nogcli.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 03 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

Preinitiation

Date of protocol fixation

2024 Year 02 Month 14 Day

Date of IRB


Anticipated trial start date

2024 Year 03 Month 05 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

This study will collect data through a web-based physician survey.
The data to be collected is indicated in the "Assessment" section.
Additionally, a prescription survey will be conducted on the continuation of treatment with tinea pedis medications.

[Prescription Survey]
The prescription survey will extract and aggregate receipt data (National Medical Data: NMD) from medical institutions contracted with the International Research Institute of Medical Strategy, Ltd.
Survey period: January 2022 - December 2023
Subjects: Patients prescribed drugs indicated for tinea pedis from January 2022 to June 2023
(Notes: patients who were prescribed a treatment indicated for tinea pedis in the 6 months immediately preceding the period are excluded.)


Management information

Registered date

2024 Year 03 Month 05 Day

Last modified on

2024 Year 03 Month 05 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000061379


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name