UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000055382 |
|---|---|
| Receipt number | R000063265 |
| Scientific Title | Verification of intestinal environment improvement by test food |
| Date of disclosure of the study information | 2025/09/01 |
| Last modified on | 2024/08/30 10:44:05 |
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Basic information
Public title
Verification of intestinal environment improvement by test food
Acronym
Verification of intestinal environment improvement by test food
Scientific Title
Verification of intestinal environment improvement by test food
Scientific Title:Acronym
Verification of intestinal environment improvement by test food
Region
| Japan |
Condition
Condition
Not applicable
Classification by specialty
| Not applicable |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To verify intestinal environment improvement function of test food
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
alteration of intensional bacterial flora
Key secondary outcomes
Bowel movement
Body weight
Base
Study type
Interventional
Study design
Basic design
Cross-over
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
Prevention
Type of intervention
| Food |
Interventions/Control_1
Test food is taken for 4 weeks
Interventions/Control_2
Placebo of control 1 is taken 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
| 65 | years-old | > |
Gender
Female
Key inclusion criteria
1) Regular visitor of Matsuike Clinic
2) Women with mild constipation who are prescribed magnesium oxide whose age at the time of obtaining consent to participate in the study is 20 to 64 years old
3) Those who have received sufficient explanation about the purpose and content of this study, have the ability to consent, volunteered to participate voluntarily after understanding well, and can agree to participate in this study in writing
4) Those who can visit the hospital on the designated day and can receive an inquiry
5) Those who are deemed appropriate by the study investigator to participate in this study
Key exclusion criteria
1) Persons with symptoms other than mild constipation
2) Persons who have no visit history for the past 3 months
3) Those who cannot be judged by the investigator without affecting the participation in the study
4) Persons with food allergies
5) Persons who habitually consume a food (regardless of manufacturer) that falls under the generic name of the test food.
6) Those who plan to become pregnant, breast-feeding, or possibly pregnant, and pregnant during the study period
8) Habitual smokers
7) Persons with alcoholism or other mental disorders
9) Persons who may change their lifestyle during the test period (night work, long trip, etc.)
10) Those who are planning to take health functional foods or supplement foods during the study period
11) Those who have been treated with hospitalization within the past 6 months
12) Persons currently participating in other human clinical trials, those who have not passed 3 months since participating in other human clinical trials
13) Other persons who are deemed inappropriate by the study investigator
Target sample size
20
Research contact person
Name of lead principal investigator
| 1st name | Naoki |
| Middle name | |
| Last name | Iemoto |
Organization
MORINAGA & CO., LTD.
Division name
R & D Center
Zip code
230-8504
Address
2-1-1 Shimosueyoshi Turumi-ku Yokohama, Kanagawa
TEL
045-571-6140
n-iemoto-jb@morinaga.co.jp
Public contact
Name of contact person
| 1st name | Ryotaro |
| Middle name | |
| Last name | Shiga |
Organization
MORINAGA & CO., LTD.
Division name
R & D Center
Zip code
230-8504
Address
2-1-1 Shimosueyoshi Turumi-ku Yokohama, Kanagawa
TEL
045-571-6140
Homepage URL
r-shiga-bb@morinaga.co.jp
Sponsor or person
Institute
MORINAGA & CO., LTD.
Institute
Department
Personal name
Funding Source
Organization
MORINAGA & CO., LTD.
Organization
Division
Category of Funding Organization
Profit organization
Nationality of Funding Organization
Other related organizations
Co-sponsor
Matsuike Clinic
Name of secondary funder(s)
IRB Contact (For public release)
Organization
Shiba Palace Clinic Ethics Review Committee
Address
DaiwaA Hamamatsucho Bldg. 6F, 1-9-10, Hamamatsucho, Minato-ku, Tokyo, 105-0013, JAPAN
Tel
03-5408-1599
shiba_palace@s-palace-clinic.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
| 2025 | Year | 09 | 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
Preinitiation
Date of protocol fixation
| 2024 | Year | 08 | Month | 07 | Day |
Date of IRB
Anticipated trial start date
| 2024 | Year | 09 | Month | 01 | Day |
Last follow-up date
| 2025 | Year | 03 | Month | 31 | 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 | 08 | Month | 30 | Day |
Last modified on
| 2024 | Year | 08 | Month | 30 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000063265
