UMIN-CTR Clinical Trial
| Unique ID issued by UMIN | UMIN000050548 |
|---|---|
| Receipt number | R000057560 |
| Scientific Title | Pilot study on the effect of test beverage on body fluid recovery from exercise-induced dehydration. |
| Date of disclosure of the study information | 2024/04/30 |
| Last modified on | 2023/05/19 13:33:16 |
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Basic information
Public title
Pilot study on the effect of test beverage on body fluid recovery from exercise-induced dehydration.
Acronym
Pilot study on the effect of test beverage on body fluid recovery from exercise-induced dehydration.
Scientific Title
Pilot study on the effect of test beverage on body fluid recovery from exercise-induced dehydration.
Scientific Title:Acronym
Pilot study on the effect of test beverage on body fluid recovery from exercise-induced dehydration.
Region
| Japan |
Condition
Condition
Healthy adult males
Classification by specialty
| Adult |
Classification by malignancy
Others
Genomic information
NO
Objectives
Narrative objectives1
To examine the effect of test beverage on body fluid recovery from exercise-induced dehydration.
Basic objectives2
Efficacy
Basic objectives -Others
Trial characteristics_1
Trial characteristics_2
Developmental phase
Assessment
Primary outcomes
Percentage changes in plasma volume
Key secondary outcomes
Urine volume
Base
Study type
Interventional
Study design
Basic design
Cross-over
Randomization
Randomized
Randomization unit
Individual
Blinding
Open -but assessor(s) 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
Control beverage -> washout period -> Test beverage
Interventions/Control_2
Test beverage -> washout period -> Control 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
| 20 | years-old | <= |
Age-upper limit
| Not applicable |
Gender
Male
Key inclusion criteria
1)Subjects who are voluntarily giving written informed consent.
2)Healthy adult males over 20 years of age.
3)Subjects who have an exercise habit (daily exercise; jogging, treadmill running, bicycle pedaling, etc.)
4)Subjects who can take meals, take blood and urine samples, and keep a resting state on the schedule indicated by investigators.
Key exclusion criteria
1)Subjects who make a blood donation of 400 ml within 12 weeks before the start of the intake or that of 200 ml within 4 weeks before the start of the intake.
2)Subjects who have or had disorder in digestive, circulatory or endocrine system and who are estimated inappropriate to this study by principal investigator.
3)Subjects who are estimated inappropriate to participate to this study by principal investigator.
Target sample size
10
Research contact person
Name of lead principal investigator
| 1st name | Shintaro |
| Middle name | |
| Last name | Ono |
Organization
Otsuka Pharmaceutical Co., Ltd
Division name
Saga Nutraceuticals Research Institute
Zip code
842-0195
Address
5006-5 Yoshinogari, Kanzaki, Saga
TEL
0952521522
Ono.Shintaro@otsuka.jp
Public contact
Name of contact person
| 1st name | Shintaro |
| Middle name | |
| Last name | Ono |
Organization
Otsuka Pharmaceutical Co., Ltd
Division name
Saga Nutraceuticals Research Institute
Zip code
842-0195
Address
5006-5 Yoshinogari, Kanzaki, Saga
TEL
0952521522
Homepage URL
Ono.Shintaro@otsuka.jp
Sponsor or person
Institute
Otsuka Pharmaceutical Co., Ltd
Institute
Department
Personal name
Funding Source
Organization
Otsuka Pharmaceutical 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
Otsuka Pharmaceutical Co., Ltd.
Address
Shinagawa Grand Central Tower, 2-16-4, Konan, Minato -ku, Tokyo
Tel
09053931433
shimizu_se@otsuka.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
大塚製薬株式会社 佐賀栄養製品研究所（佐賀県）
Other administrative information
Date of disclosure of the study information
| 2024 | Year | 04 | Month | 30 | 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
| 2023 | Year | 03 | Month | 08 | Day |
Date of IRB
| 2023 | Year | 03 | Month | 09 | Day |
Anticipated trial start date
| 2023 | Year | 03 | Month | 13 | Day |
Last follow-up date
| 2023 | Year | 04 | 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
| 2023 | Year | 03 | Month | 09 | Day |
Last modified on
| 2023 | Year | 05 | Month | 19 | Day |
Link to view the page
Value
https://center6.umin.ac.jp/cgi-open-bin/ctr_e/ctr_view.cgi?recptno=R000057560
