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The Development of the Intravenous Drip Management System by the ICT Utilization

semi-experimental study - semi-experimental study

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000036423
Enrollment
30
Registered
2019-06-01
Start date
2019-06-01
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

Patients receiving fluid therapy

Interventions

Nurses manages of intravenous drip with the system mobile. Nurses manages of intravenous drip without the system mobile.

Sponsors

Kumamoto University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: The patients that circulation status and respiratory status are stable, and the patients who got permission of the chief physician.

Exclusion criteria

Exclusion criteria: The patients that circulation status and respiratory status are unstable, and the disturbed patient by delirium and dementia.

Design outcomes

Primary

MeasureTime frame
The difference of intravenous drip doses per one hour by the presence or absence of system utilization

Countries

Japan

Contacts

Public ContactChiahru Matsumoto

Kumamoto University Department of Nursing, Faculty of Life Sciences

matsu-c@kumamoto-u.ac.jp096-373-5517

Outcome results

None listed

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