UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000012511
Receipt number R000014627
Scientific Title An immunohistological study of the human skin before and after application of cosmetic lotions containing various molecular sizes of hyaluronan and a supplementary study about ability of steroid production in epidermis by application of ACTH.
Date of disclosure of the study information 2013/12/31
Last modified on 2014/11/13 22:16:18

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Basic information

Public title

An immunohistological study of the human skin before and after application of cosmetic lotions containing various molecular sizes of hyaluronan and a supplementary study about ability of steroid production in epidermis by application of ACTH.

Acronym

Immunohistological changes of human skin by hyaluronan lotion and the epidermis ACTH loading test.

Scientific Title

An immunohistological study of the human skin before and after application of cosmetic lotions containing various molecular sizes of hyaluronan and a supplementary study about ability of steroid production in epidermis by application of ACTH.

Scientific Title:Acronym

Immunohistological changes of human skin by hyaluronan lotion and the epidermis ACTH loading test.

Region

Japan


Condition

Condition

1.aged skin
2.atopic dermatitis

Classification by specialty

Dermatology Aesthetic surgery

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To confirm the effect of hyaluronan lotion application to 1) aged skin 2) atopic dermatitis. To confirm steroid production ability of epidermis at the same time in the latter in which the effect might be different according to topical steroid application.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

Immunohistological changes before and after application of hyaluronan lotion for two weeks.

Key secondary outcomes

Immunohistological changes before and after application of ACTH lotion for two weeks.


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


Institution consideration


Blocking


Concealment



Intervention

No. of arms

1

Purpose of intervention

Treatment

Type of intervention

Other

Interventions/Control_1

External application of hyaluronan lotion twice a day for two weeks.
External application of ACTH solution also twice a day for two weeks in patients with atopic dermatitis.

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

Eligible over 60 years old in aged skin subjects.

Key exclusion criteria

Ineligible under 60 years old in aged skin subjects.

Target sample size

20


Research contact person

Name of lead principal investigator

1st name
Middle name
Last name Mototsugu Fukaya

Organization

Tsurumai Kouen Clinic

Division name

Cosmetic surgery and dermatology

Zip code


Address

5-20-6 Choyoda Nakaku Nagoya 460-0012 Japan

TEL

+81-52-264-0212

Email

moto@earth.ocn.ne.jp


Public contact

Name of contact person

1st name
Middle name
Last name Mototsugu Fukaya

Organization

Tsurumai Kouen Clinic

Division name

Cosmetic surgery and dermatolgy

Zip code


Address

5-20-6 Choyoda Nakaku Nagoya 460-0012 Japan

TEL

+81-52-264-0212

Homepage URL


Email

moto@earth.ocn.ne.jp


Sponsor or person

Institute

Tsurumai Kouen Clinic

Institute

Department

Personal name



Funding Source

Organization

Tsurumai Kouen Clinic

Organization

Division

Category of Funding Organization

Self funding

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization


Address


Tel


Email



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

2013 Year 12 Month 31 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications

http://www.scirp.org/journal/PaperInformation.aspx?PaperID=46333

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

Completed

Date of protocol fixation

2013 Year 11 Month 28 Day

Date of IRB


Anticipated trial start date

2014 Year 01 Month 01 Day

Last follow-up date


Date of closure to data entry

2014 Year 11 Month 13 Day

Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2013 Year 12 Month 06 Day

Last modified on

2014 Year 11 Month 13 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000014627


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name