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Comparison of Ease of Use of Three Drug Infusion Pumps in Neonatal Intensive Care Unit: A retrospective study.

Comparison of Ease of Use of Three Drug Infusion Pumps in Neonatal Intensive Care Unit: A retrospective Study

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
CRIS
Registry ID
KCT0004613
Enrollment
90
Registered
2020-01-07
Start date
2019-09-04
Completion date
Unknown
Last updated
2020-06-15

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

Conditions

None listed

Interventions

None listed

Sponsors

Meinntech
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Those who have been in the neonatal intensive care unit and have used a syringe pump or a cylinder pump (Horizon type). 2) Those who have received main fluid or TPN for more than 24 hours through a syringe pump or a cylinder pump.

Exclusion criteria

Exclusion criteria: None.

Design outcomes

Primary

MeasureTime frame
Time to prepare for each pump (min), exposure time of the set of fluid or syringe for 24 hours per pump (sec)—

Secondary

MeasureTime frame
Cartridge or syringe replacements for 24 hours per pump, Alarms generated for 24 hours per pump—

Countries

Korea, Republic of

Contacts

Public ContactYu Kim

Gachon University Gil Medical Center

Outcome results

None listed

Source: CRIS (via WHO ICTRP) · Data processed: Feb 4, 2026