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tility of new muscular flaccidity monitorTOFCuff

Not Applicable
Conditions
The operation patient who needs general anesthesia 15 years or older
Registration Number
JPRN-UMIN000024968
Lead Sponsor
Sapporo medical university hospital, Department of Anesthesiology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
40
Inclusion Criteria

Not provided

Exclusion Criteria

Patient younger than 15 years Patient having a neuromuscular disease Patient having a renal function disorder Patient having a liver function disorder Patient thought to be the skin state having difficulty in line relaxation monitoring The patient whom a study representative or an allotment researcher judged not to be able to evaluate it who it is not cooperative or is enough after a study start during a period until leaving In addition, the patient who judged that a study representative or an allotment researcher was inappropriate

Study & Design

Study Type
Interventional
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Correlation of the line relaxation monitoring in TOF-Watch and TOFCuff
Secondary Outcome Measures
NameTimeMethod
Having or not early post operation respiratory dysfunction
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