UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000034215
Receipt number R000039007
Scientific Title Effect of lactic acid bacteria consumption on moisture in skin of healthy females: the pilot study.
Date of disclosure of the study information 2019/09/19
Last modified on 2020/06/30 15:06:10

* This page includes information on clinical trials registered in UMIN clinical trial registed system.
* We don't aim to advertise certain products or treatments


Basic information

Public title

Effect of lactic acid bacteria consumption on moisture in skin of healthy females: the pilot study.

Acronym

Effect of lactic acid bacteria consumption on skin of healthy females.

Scientific Title

Effect of lactic acid bacteria consumption on moisture in skin of healthy females: the pilot study.

Scientific Title:Acronym

Effect of lactic acid bacteria consumption on skin of healthy females.

Region

Japan


Condition

Condition

Healthy adults

Classification by specialty

Dermatology

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To clarify the effect of intake of lactic acid bacteria on skin moisture.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Exploratory

Trial characteristics_2

Explanatory

Developmental phase

Not applicable


Assessment

Primary outcomes

Water content of stratum corneum, and moisture transpiration.

Key secondary outcomes

1. Concentration of phenolic compound in feces.
2. Construction of fecal micro biota.


Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification

YES

Dynamic allocation

YES

Institution consideration

Institution is not considered as adjustment factor.

Blocking

YES

Concealment

Central registration


Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Food

Interventions/Control_1

Intake of lactic acid beverage

Interventions/Control_2

Intake of placebo beverage

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

18 years-old <=

Age-upper limit

65 years-old >=

Gender

Female

Key inclusion criteria

Who have subjective symptoms of dry skin

Key exclusion criteria

1. Who have any skin disease
2. Who have any serious illness, for example, heart disease, kidney disease, diabetes mellitus, and so on.
3. Who take any medicine which effect intestinal flora, such as antibiotics.
4. Who have allergic to apple, soy bean, dairy food.
5. Who expose to high-intensity ultraviolet rays.
6. Who are pregnant or breast-feeding or willing to be pregnant during this study.
7. Who have receive medical treatments for gastrointestinal diseases that affect regulation of intestinal function, or a history of those (except for appendicectomy).
8. Who have participated in other clinical study for skin during this study, or willing to be that.
9. Who are eating an unbalanced diet, such as binge eating, and fasting.
10, Who are judged unsuitable for this study by principal investigator.

Target sample size

60


Research contact person

Name of lead principal investigator

1st name Shigenori
Middle name
Last name Suzuki

Organization

Kagome Co. Ltd.

Division name

Nature & Wellness Research Department

Zip code

329-2762

Address

17 Nishitomiyama, Nasushiobara city, Tochigi

TEL

0287-36-2935

Email

Shigenori_Suzuki@kagome.co.jp


Public contact

Name of contact person

1st name Naoko
Middle name
Last name Waki

Organization

Kagome Co. Ltd.

Division name

Nature & Wellness Research Department

Zip code

329-2762

Address

17 Nishitomiyama, Nasushiobara city, Tochigi

TEL

0287-36-2935

Homepage URL


Email

Naoko_Waki@kagome.co.jp


Sponsor or person

Institute

Kagome Co. Ltd.

Institute

Department

Personal name



Funding Source

Organization

Kagome Co. Ltd.

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor

Showa Women's University

Name of secondary funder(s)



IRB Contact (For public release)

Organization

Kagome Ethics Committee

Address

3-21-1, F tower, Hamacho, Nihonbashi, Tyuo-ku, Tokyo, Japan

Tel

03-5623-8501

Email

Takuji_Hayakawa@kagome.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

昭和女子大学(東京都)


Other administrative information

Date of disclosure of the study information

2019 Year 09 Month 19 Day


Related information

URL releasing protocol


Publication of results

Published


Result

URL related to results and publications


Number of participants that the trial has enrolled

70

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

Main results already published

Date of protocol fixation

2018 Year 08 Month 31 Day

Date of IRB

2018 Year 08 Month 31 Day

Anticipated trial start date

2018 Year 10 Month 27 Day

Last follow-up date

2019 Year 06 Month 30 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information



Management information

Registered date

2018 Year 09 Month 20 Day

Last modified on

2020 Year 06 Month 30 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000039007


Research Plan
Registered date File name

Research case data specifications
Registered date File name

Research case data
Registered date File name