Examination of the hydration effect with the oral rehydration water

Examination of the hydration effect with the oral rehydration water - Examination of the hydration effect with the oral rehydration water

Status

Active, not recruiting

Phases

Phase 1

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000018417

Enrollment

Registered

2015-07-24

Start date

2013-12-15

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 volunteer

Interventions

fasting-&gt

wash out period-&gt

drinking-oral rehydration solution-&gt

intravenous drip fasting-&gt

intravenous drip

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: The person that I made a medical examination before an examination, and abnormality was not recognized

Exclusion criteria

Exclusion criteria: Person having diabetes. Person having the disease of the cardiovascular system. Person having hyperthyroidism. Person having a severe liver function disorder, renal function disorder. The person who judged that the medical attendant of this study was inappropriate.

Design outcomes

Primary

Measure	Time frame
Before and after of the oral rehydration water	—

Countries

Japan

Contacts

Public ContactShigeki Fujiwara

Kyushu university Dental anesthesiology

fujiwara@dent.kyushu-u.ac.jp092-642-6480

Outcome results

None listed

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