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Comparison of operator workloads during a changeover of continuous infusion from syringe pump to infusion pump

Conditions
Not Applicable
Registration Number
KCT0004172
Lead Sponsor
Korea Health Industry Development Institute
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot yet recruiting
Sex
All
Target Recruitment
22
Inclusion Criteria

participants who receive a 2-hour practical demonstration of operation with the relevant devices, followed by a 4-week training course including practical work

Exclusion Criteria

not applicable.

Study & Design

Study Type
Observational Study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
total execution time, defined as time taken from the setup with a syringe pump mode to the administration of the medication via a changed infusion pump mode.
Secondary Outcome Measures
NameTimeMethod
total number of clicks;subjective difficulty score using a numerical rating scale with a score from 0 (extremely easy) to 10 (extremely difficult)
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