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Frequency and the risk factors of ICU-AW after critical illness

Not Applicable
Recruiting
Conditions
ICU acquired weakness
Registration Number
JPRN-UMIN000030471
Lead Sponsor
Sapporo Medical University School of Medicene, Department of Intensive Care Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
50
Inclusion Criteria

Not provided

Exclusion Criteria

The patients who didn't got agreement on this study The patients judged as inappropriate enrollment

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
the rate of ICU-AW and the time when nerve conduction study has changed
Secondary Outcome Measures
NameTimeMethod
prognosis(ICU, 28day, 90day, hospital mortality) inflamatory biomarker(CRP, Procalcitonin, Presepsin) Plasma cytokine(IL-1, IL-4, IL-6, IL-8, IL-10, IFN-gamma, TNF-alpha) Steroid, Immunoglobulin, Sedatives day of the beginning of rehabilitation, period of rehabilitation
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