UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000054478
Receipt number R000062225
Scientific Title Evaluation test of composition 240415 for oral cavity
Date of disclosure of the study information 2024/06/01
Last modified on 2026/01/20 16:32:42

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Basic information

Public title

Use test of the toothpaste

Acronym

Use test of the toothpaste

Scientific Title

Evaluation test of composition 240415 for oral cavity

Scientific Title:Acronym

Evaluation test for oral cavity

Region

Japan


Condition

Condition

Not applicable

Classification by specialty

Not applicable Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To examine the efficacy of composition 240415 for oral cavity

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase

Not applicable


Assessment

Primary outcomes

Measurement of oral index.
Measurements are taken 3 times, before starting test, after using composion 240415 for 12 weeks and 24 weeks.

Key secondary outcomes



Base

Study type

Interventional


Study design

Basic design

Parallel

Randomization

Randomized

Randomization unit

Individual

Blinding

Double blind -all involved are blinded

Control

Placebo

Stratification


Dynamic allocation


Institution consideration


Blocking


Concealment



Intervention

No. of arms

2

Purpose of intervention

Treatment

Type of intervention

Behavior,custom

Interventions/Control_1

Brushing teeth with oral composition 240415 for 24 weeks.

Interventions/Control_2

Brushing teeth with placebo composition for 24 weeks.

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

40 years-old <=

Age-upper limit

65 years-old >=

Gender

Male and Female

Key inclusion criteria

-Male or female of 40 to 65 years of age
-1 or 2, and 3 or 4 or 5
1.Subjects who feel that their gums are falling and their teeth are getting longer.
2.Subjects who feel that food gets stuck between their teeth.
3.Subjects who may bleed from gingival.
4.Subjects with occasional swelling of gingival.
5.Subjects have been diagnosed with swollen gingival or deep periodontal pockets.
-Subjects who have 20 or more of their own teeth.
-Subjects who brush their teeth at
least twice a day.

Key exclusion criteria

-Subjects with systemic illness.
-Subjects who are taking prescription medicine (except for anti-hay fever).
-Subjects with a disease in the oral cavity and are consulting the medical institution.
-Subjects undergoing treatment for periodontal disease
-Subjects undergoing orthodontic therapy.
-Subjects with mobile tooth.
-Subjects with an implant
-Subjects who have regular dental checkups at least 3 times a year.
-The pregnant and subjects who hope to get pregnant during the exam period.
-Subjects with smoking habit
-Subjects who participate in the other examinations.
-Subjects from outside the company who work in an advertising agency, an investigation, consultancy, mass communication, and the manufacturing industry of health food, cosmetics, toiletries, a sanitary items, and a distributive trade.
-Subjects deemed inappropriate to participate in this study by the principle investigator.

Target sample size

46


Research contact person

Name of lead principal investigator

1st name Atsuko
Middle name
Last name Hayase

Organization

Kao Corporation

Division name

Biological Science Research Lab.

Zip code

321-3497

Address

2606, Akabane, Ichikai-Machi, Haga-Gun Tochigi, 321-3497, JAPAN

TEL

+81-285-68-7236

Email

hayase.atsuko@kao.com


Public contact

Name of contact person

1st name Hatsumi
Middle name
Last name Souno

Organization

Kao Corporation

Division name

Biological Science Research Lab.

Zip code

321-3497

Address

2606, Akabane, Ichikai-Machi, Haga-Gun Tochigi, 321-3497, JAPAN

TEL

+81-3-5630-9064

Homepage URL


Email

souno.hatsumi@kao.com


Sponsor or person

Institute

Kao Corporation

Institute

Department

Personal name



Funding Source

Organization

Kao Corporation

Organization

Division

Category of Funding Organization

Profit organization

Nationality of Funding Organization



Other related organizations

Co-sponsor


Name of secondary funder(s)



IRB Contact (For public release)

Organization

Human Research Ethics Committee, Kao Corporation

Address

2-1-3 Bunka, Sumida-ku, Tokyo 131-8501, JAPAN

Tel

+81-3-5630-9064

Email

morisaki.naoko@kao.com


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 06 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

Completed

Date of protocol fixation

2024 Year 05 Month 14 Day

Date of IRB

2024 Year 05 Month 14 Day

Anticipated trial start date

2024 Year 07 Month 10 Day

Last follow-up date

2025 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

2024 Year 05 Month 24 Day

Last modified on

2026 Year 01 Month 20 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000062225