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Clinical implementation of the infusion rate individualization of intravenous lipid emulsion

Clinical implementation of the infusion rate individualization of soybean oil-based intravenous lipid emulsion: A multi-center descriptive cohort study - Clinical implementation of the infusion rate individualization of intravenous lipid emulsion

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000054236
Enrollment
120
Registered
2024-04-24
Start date
2023-11-01
Completion date
Unknown
Last updated
2026-09-14

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

Conditions

Patients who clinically need intravenous lipid emulsion

Interventions

None listed

Sponsors

Kobe Gakuin University
Lead Sponsor
Ageo Central General Hospital Joetsu GeneralHospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Baseline triglyceride level < 300 mg/dL

Exclusion criteria

Exclusion criteria: Patients with estimated individualized infusion rates less than 10 mL/h or greater than 0.33 g/kg/h

Design outcomes

Primary

MeasureTime frame
Maximum triglyceride concentration on the final day of administration

Secondary

MeasureTime frame
Laboratory parameters, including liver function, renal function, and markers of inflammation

Countries

Japan

Contacts

Public ContactKeizo Fukushima

Kobe Gakuin University Faculty of Pharmaceutical Sciences

keizo@pharm.kobegakuin.ac.jp078-974-4441

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Sep 19, 2026