UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000026469
Receipt number R000029299
Scientific Title Clinical study of heparinoid for sweating response in healthy volunteer.
Date of disclosure of the study information 2017/04/01
Last modified on 2023/10/16 11:30:23

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Basic information

Public title

Clinical study of heparinoid for sweating response in healthy volunteer.

Acronym

Clinical study of heparinoid for sweating response

Scientific Title

Clinical study of heparinoid for sweating response in healthy volunteer.

Scientific Title:Acronym

Clinical study of heparinoid for sweating response

Region

Japan


Condition

Condition

healthy control

Classification by specialty

Dermatology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

Analysis of sweating response associated with heparinoid containing moisturizer.

Basic objectives2

Others

Basic objectives -Others

efficacy for sweating response

Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

Status of sweating after application for 2 weeks.

Key secondary outcomes

Skin surface hydration, texture of skin.


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Non-randomized

Randomization unit


Blinding

Open -but assessor(s) are blinded

Control

Placebo

Stratification

NO

Dynamic allocation

NO

Institution consideration

Institution is not considered as adjustment factor.

Blocking

NO

Concealment

Numbered container method


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Medicine

Interventions/Control_1

moisturizer and base.

Interventions/Control_2

7 days and 14 days.

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.Person older than 20yo.
2.Person who agree to participate in this trial.
3.Healthy person.

Key exclusion criteria

1.Person with allergic dermatitis.
2.Person with sweat disturbance.
3.Person who has hypersensitivity for moisturizer and base.
4.Person who enrolled in other clinical trial within a month.
5.Person who was disqualified by principal clinician.

Target sample size

30


Research contact person

Name of lead principal investigator

1st name Yumi
Middle name
Last name Aoyama

Organization

Department of dermatology, Kawasaki Medical School, 577 Matsushima Kurashiki city, Okayama Japan

Division name

Dermatology

Zip code

701-0192

Address

086-225-2111

TEL

086-462-1111

Email

ymaoyama@med.kawasaki-m.ac.jp


Public contact

Name of contact person

1st name Yumi
Middle name
Last name Aoyama

Organization

Department of dermatology, Kawasaki Medical School, 577 Matsushima Kurashiki city, Okayama Japan

Division name

Dermatology

Zip code

701-0192

Address

086-225-2111

TEL

086-462-1111

Homepage URL


Email

ymaoyama@med.kawasaki-m.ac.jp


Sponsor or person

Institute

Department of dermatology, Kawasaki Medical School, 577 Matsushima Kurashiki city, Okayama Japan

Institute

Department

Personal name



Funding Source

Organization

Kawasaki Medical School

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

Kawasaki Medical School

Address

577 Matsushima Kurashiki Japan

Tel

086-462-1111

Email

kmsrec@med.kawasaki-m.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

2017 Year 04 Month 01 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

Open public recruiting

Date of protocol fixation

2017 Year 03 Month 01 Day

Date of IRB

2018 Year 04 Month 09 Day

Anticipated trial start date

2019 Year 04 Month 01 Day

Last follow-up date

2025 Year 03 Month 31 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Monitoring on February 19, 2021
February 2022 No people subject to monitoring
August 2022 No monitoring targets
February 2023 No people subject to monitoring


Management information

Registered date

2017 Year 03 Month 09 Day

Last modified on

2023 Year 10 Month 16 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000029299


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name