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Blood concentration of propofol in pregnant women during target controlled infusion (TCI)

Not Applicable
Recruiting
Conditions
pregnancy
Registration Number
JPRN-UMIN000015801
Lead Sponsor
iigata University Medical & Dental Hospital Department of Anesthesiology
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
Female
Target Recruitment
6
Inclusion Criteria

Not provided

Exclusion Criteria

Minority Those who were not able to get consent to an inspection A 30 or more-BMI person

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The difference between the blood levels of the measured and predicted blood concentration of propofol in a pregnant woman
Secondary Outcome Measures
NameTimeMethod
A propofol infusion dose required in order to maintain proper stillness
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