UMIN ID: UMIN000054236
Registered date:24/04/2024
Clinical implementation of the infusion rate individualization of intravenous lipid emulsion
Basic Information
Recruitment status | Recruiting |
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Health condition(s) or Problem(s) studied | Patients who clinically need intravenous lipid emulsion |
Date of first enrollment | 2023/11/01 |
Target sample size | 120 |
Countries of recruitment | Japan |
Study type | Observational |
Intervention(s) |
Outcome(s)
Primary Outcome | Maximum triglyceride concentration on the final day of administration |
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Secondary Outcome | Laboratory parameters, including liver function, renal function, and markers of inflammation |
Key inclusion & exclusion criteria
Age minimum | 18years-old |
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Age maximum | Not applicable |
Gender | Male and Female |
Include criteria | |
Exclude criteria | Patients with estimated individualized infusion rates less than 10 mL/h or greater than 0.33 g/kg/h |
Related Information
Primary Sponsor | Kobe Gakuin University |
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Secondary Sponsor | Ageo Central General Hospital Joetsu GeneralHospital |
Source(s) of Monetary Support | Kobe Gakuin University |
Secondary ID(s) |
Contact
public contact | |
Name | Keizo Fukushima |
Address | 1-1-3 Minatojima, Chuo district, Kobe city, Hyogo prefecture, Japan Japan 650-8586 |
Telephone | 078-974-4441 |
keizo@pharm.kobegakuin.ac.jp | |
Affiliation | Kobe Gakuin University Faculty of Pharmaceutical Sciences |
scientific contact | |
Name | Keizo Fukushima |
Address | 1-1-3 Minatojima, Chuo district, Kobe city, Hyogo prefecture, Japan Japan |
Telephone | 078-974-4441 |
keizo@pharm.kobegakuin.ac.jp | |
Affiliation | Kobe Gakuin University Faculty of Pharmaceutical Sciences |