UMIN-CTR Clinical Trial

Unique ID issued by UMIN UMIN000038173
Receipt number R000043068
Scientific Title Effect of lactic acid bacteria beverage on bowel movement
Date of disclosure of the study information 2019/10/01
Last modified on 2022/04/04 15:27:02

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Basic information

Public title

Effect of lactic acid bacteria beverage on bowel movement

Acronym

Effect of lactic acid bacteria beverage on bowel movement

Scientific Title

Effect of lactic acid bacteria beverage on bowel movement

Scientific Title:Acronym

Effect of lactic acid bacteria beverage on bowel movement

Region

Japan


Condition

Condition

Healthy

Classification by specialty

Adult

Classification by malignancy

Others

Genomic information

NO


Objectives

Narrative objectives1

To assess the effect of Lactobacillus plantarum SN13T-fermented beverage on bowel movement and fecal microbiota.

Basic objectives2

Efficacy

Basic objectives -Others


Trial characteristics_1

Confirmatory

Trial characteristics_2

Pragmatic

Developmental phase

Not applicable


Assessment

Primary outcomes

4-week change in defecation frequency

Key secondary outcomes

4-week changes in fetal microbiota, questionnaire about bowel movement (abdominal pain, feeling of incomplete evacuation, form, volume, and odor), serum AST, ALT, and r-GTP


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

NO

Institution consideration


Blocking

YES

Concealment

No need to know


Intervention

No. of arms

2

Purpose of intervention

Prevention

Type of intervention

Food

Interventions/Control_1

Subjects drink 100 mL/day of Lactobacillus plantarum SN13T-fermented beverage for 4 weeks.

Interventions/Control_2

Subjects drink 100 mL/day of placebo beverage for 4 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

20 years-old <=

Age-upper limit

75 years-old >=

Gender

Male and Female

Key inclusion criteria

1) Healthy
2) Defecation frequency <=3 times/week
3) Willing to provide written informed consent

Key exclusion criteria

1) Taking medicines for chronic disease
2) Taking medicines or functional food that may affect the trial
3) Participation in any clinical trial within 90 days of the commencement of the trial
4) In pregnancy or nursing a child
5) Judged as ineligible by clinical investigators

Target sample size

60


Research contact person

Name of lead principal investigator

1st name Fumiko
Middle name
Last name Higashikawa

Organization

Graduate School of Biomedical and Health Sciences, Hiroshima University

Division name

Department of Probiotic Science for Preventive Medicine

Zip code

734-8551

Address

Kasumi 1-2-3, Minami-ku, Hiroshima

TEL

082-257-1533

Email

fumiko@hiroshima-u.ac.jp


Public contact

Name of contact person

1st name Fumiko
Middle name
Last name Higashikawa

Organization

Graduate School of Biomedical and Health Sciences, Hiroshima University

Division name

Department of Probiotic Science for Preventive Medicine

Zip code

734-8551

Address

Kasumi 1-2-3, Minami-ku, Hiroshima

TEL

082-257-1533

Homepage URL


Email

funcfood@hiroshima-u.ac.jp


Sponsor or person

Institute

Hiroshima University

Institute

Department

Personal name



Funding Source

Organization

Nomura Dairy Products Co., Ltd.

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 Ethics Review Committee of Hiroshima University

Address

Kasumi 1-2-3, Minami-ku, Hiroshima

Tel

082-257-5907

Email

kasumi-kenkyu@office.hiroshima-u.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

広島大学病院(広島県)


Other administrative information

Date of disclosure of the study information

2019 Year 10 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

60

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

2019 Year 09 Month 30 Day

Date of IRB

2019 Year 09 Month 30 Day

Anticipated trial start date

2019 Year 10 Month 20 Day

Last follow-up date

2022 Year 02 Month 28 Day

Date of closure to data entry


Date trial data considered complete


Date analysis concluded

2022 Year 03 Month 31 Day


Other

Other related information



Management information

Registered date

2019 Year 10 Month 01 Day

Last modified on

2022 Year 04 Month 04 Day



Link to view the page

Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000043068