Standardization of Body fluid evaluation in Specified Medical Acts using body composition analyzer and its application for the training of nurses completing the educational program.

Standardization of Body fluid evaluation in Specified Medical Acts using body composition analyzer and its application for the training of nurses completing the educational program. - Standardization of Body fluid evaluation in Specified Medical Acts using body composition analyzer and its application for the training of nurses completing the educational program.

Status

Active, not recruiting

Phases

Unknown

Study type

Interventional

Source

JPRN

Registry ID

JPRN-UMIN000044828

Enrollment

Registered

2021-10-01

Start date

2021-09-01

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

dehydration

Interventions

Evaluate body fluid volume using bioimpedance method. This step will be applied only one time for each evaluation when planning an infusion plan.

Eligibility

Sex/Gender

All

Inclusion criteria

Inclusion criteria: Patients who meet all of the following criteria. 1) Disease name and diagnostic method: Patients with suspected or potentially dehydrated dehydration 2) Provisions for stage, type, and pathology: Evaluate the patient's condition according to the procedure manual for specific actions specified separately, confirm that the patient condition is within the scope of the procedure manual, and include it in the target. 3) Age: Patients aged 20 years or older at the time of consent acquisition 4) Gender: Gender does not matter 5) Indicators of general condition: vital signs, stable respiratory and circulatory dynamics 6) Related major organ functions: Heart function and renal function are maintained 7) Written consent of the research subject or surrogate: Patients who have voluntarily consented to the document

Exclusion criteria

Exclusion criteria: Patients who fall under any of the following will not be included in this study. 1) Conditions related to heart disease: Concomitant with unstable angina or a history of myocardial infarction within 6 months. Patients with heart failure symptoms 2) Women who are pregnant or may become pregnant 3) Implants with conductive implants such as pacemakers 4) When the principal investigator and the research coordinator judge that participation in this research is not appropriate

Design outcomes

Primary

Measure	Time frame
To establish the objective index by using a body composition analyzer to the evaluation of body fluid volume by comparing it with the evaluation by physical findings and conventional laboratory findings.	—

Secondary

Measure	Time frame
To improve the accuracy of fluid volume evaluation in specific actions of nurses by utilizing the objective index of the body composition analyzer.	—

Countries

Japan

Contacts

Public ContactTakamoto Ohse

JCHO Tokyo Shinjuku Medical Center Division of Nephrology

toose-tky@umin.ac.jp03-3269-8111

Outcome results

None listed

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