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

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

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
JPRN
Registry ID
JPRN-UMIN000015801
Enrollment
6
Registered
2015-03-01
Start date
2014-10-15
Completion date
Unknown
Last updated
2026-06-29

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

Conditions

pregnancy

Interventions

None listed

Sponsors

Niigata University Medical & Dental Hospital Department of Anesthesiology
Lead Sponsor

Eligibility

Sex/Gender
Female

Inclusion criteria

Inclusion criteria: A propofol maintenance given dose required in order to maintain proper stillness

Exclusion criteria

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

Design outcomes

Primary

MeasureTime frame
The difference between the blood levels of the measured and predicted blood concentration of propofol in a pregnant woman

Secondary

MeasureTime frame
A propofol infusion dose required in order to maintain proper stillness

Countries

Japan

Contacts

Public ContactMisako Takamatsua

Central operation part Department of anesthesia

misakotaka@gmail.com025-227-2328

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026