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Verification of the effects of ORS intake on urination during dehydration after exercise.

Verification of the effects of ORS intake on urination during dehydration after exercise.: Open-label crossover comparative study - Verification of the effects of ORS intake on urination during dehydration after exercise.: Open-label crossover comparative study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000057166
Enrollment
10
Registered
2025-02-28
Start date
2025-03-01
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Healthy adults

Interventions

Consumption of test food Consumption of control food

Sponsors

Miura Clinic, Medical Corporation Kanonkai
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Subjects of men and women aged 18 to 30 (2) Subjects who received sufficient explanation about the purpose and content of the test, had the ability to consent, voluntarily volunteered to participate after understanding it well, and agreed to participate in the test in writing.

Exclusion criteria

Exclusion criteria: (1) Subjects with a history of diabetes mellitus, liver disease, renal disease, gastrointestinal disease, cardiac disease, respiratory disease, peripheral vascular disease, or other serious diseases. (2) Subjects who have undergone gastrointestinal surgery (3) Subjects showing abnormal liver and kidney function test values. (4) Subjects who are allergic to food and drugs (5) Subjects with anemia symptoms (6) Female subjects wishing to become pregnant while participating in this study, pregnant (including those who may be pregnant) or lactating female subjects (7) Subjects with extremely irregular eating habits (8) Subjects who cannot stop taking health foods (including foods for specified health use and foods with functional claims) and quasi-drugs during the study period (9) Subjects who are continuously treated with medications (including OTC, prescription drugs) (10) Subjects who drink more than 40g of ayarage daily pure alcohol (11) Subjects who smoke an average of 21 or more cigarettes a day (12) Subjects who are currently participating in other clinical studies or are scheduled to participate in research at the start of this study. (13) Other subjects judged by the investigator or the investigator to be inappropriate for the examination

Design outcomes

Primary

MeasureTime frame
Total urine volume at the end of the observation period.

Secondary

MeasureTime frame
Body weight Body temperature Amount of sweating Serum osmolality

Countries

Japan

Contacts

Public ContactMakoto Terashima

Oneness Support Co., Ltd. Clinical Trial Division

mterashima@oneness-sup.co.jp06-4801-8917

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026