UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000056914
Receipt number R000065043
Scientific Title Efficacy of L.reuteri Prodentis(Limosilactobacillus reuteri DSM 17938 and Limosilactobacillus reuteri ATCC PTA 5289) on oral environment in healthy adults:A systematic review
Date of disclosure of the study information 2025/02/07
Last modified on 2025/02/03 11:30:04

* 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

Efficacy of L.reuteri Prodentis on oral environment:A systematic review

Acronym

Efficacy of L.reuteri Prodentis on oral environment:A systematic review

Scientific Title

Efficacy of L.reuteri Prodentis(Limosilactobacillus reuteri DSM 17938 and Limosilactobacillus reuteri ATCC PTA 5289) on oral environment in healthy adults:A systematic review

Scientific Title:Acronym

Efficacy of L.reuteri Prodentis(Limosilactobacillus reuteri DSM 17938 and Limosilactobacillus reuteri ATCC PTA 5289) on oral environment in healthy adults:A systematic review

Region

Japan


Condition

Condition

Healthy adults

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

The purpose of this study was to verify whether ingestion of L. reuteri Prodentis by healthy adults has an ameliorative effect on the oral environment.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1


Trial characteristics_2


Developmental phase



Assessment

Primary outcomes

oral flora, gums

Key secondary outcomes



Base

Study type

Others,meta-analysis etc


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

18 years-old <=

Age-upper limit


Not applicable

Gender

Male and Female

Key inclusion criteria

Studies that meet the following PICOS and conditions
P: healthy adults
I: Foods containing L.reuteri Prodentis
C: Foods not containing L.reuteri Prodentis
O: Improvement of oral environment
S: Randomized controlled trial or equivalent

Languages : English, Japanese
Publication status : Original peer-reviewed paper

Key exclusion criteria

-Examination for the following persons : patient, expectant and nursing mothers
-Studies using test products that contain ingredients other than L.reuteri Prodentis that affect test results.
-in vivo, in vitro

Target sample size



Research contact person

Name of lead principal investigator

1st name Hisashi
Middle name
Last name Takeuchi

Organization

Association of Japan CAM

Division name

N/A

Zip code

151-0053

Address

#306 Onogibiru,3-46-16 Yoyogi, Shibuya-ku, Tokyo

TEL

03-6457-4911

Email

info@ajcam.biz


Public contact

Name of contact person

1st name Takeshi
Middle name
Last name Kaneko

Organization

Japan Clinical Trial Association

Division name

N/A

Zip code

1600022

Address

5F, 4-3-17 Shinjuku, Shinjukuku, Tokyo

TEL

0364574666

Homepage URL


Email

info@yakujihou.org


Sponsor or person

Institute

Japan Clinical Trial Association

Institute

Department

Personal name



Funding Source

Organization

BioGaia Japan INC.

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

Japan Clinical Trial Association

Address

5F, 4-3-17 Shinjuku, Shinjukuku, Tokyo

Tel

0364574666

Email

info@yakujihou.org


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

2025 Year 02 Month 07 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

2025 Year 02 Month 07 Day

Date of IRB


Anticipated trial start date

2025 Year 02 Month 07 Day

Last follow-up date

2026 Year 02 Month 07 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded



Other

Other related information

Literature database
-PubMed
-JDream3
-Cochrane Library


Management information

Registered date

2025 Year 02 Month 03 Day

Last modified on

2025 Year 02 Month 03 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000065043