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The Effective Effect-Site Propofol Concentration for Induction and Intubation for Schnider model using total body weight in parturients

The Effective Effect-Site Propofol Concentration for Induction and Intubation for Schnider model using total body weight in parturients

Status
Active, not recruiting
Phases
Unknown
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR-OOR-16009313
Enrollment
Unknown
Registered
2016-10-04
Start date
2016-10-15
Completion date
Unknown
Last updated
2017-04-18

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

Conditions

caesarean section

Interventions

6 groups:predetermined target propofol Ce in different concentration

Sponsors

Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China
Lead Sponsor

Eligibility

Sex/Gender
Female
Age
18 Years to 45 Years

Inclusion criteria

Inclusion criteria: undergoing elective cesarean section under general anesthesia were enrolled in this prospective observational study

Exclusion criteria

Exclusion criteria: diabetes controlled by insulin, preeclampsia, heart diseases, and history of taking drugs potentially affecting cardiovascular system.

Design outcomes

Primary

MeasureTime frame
effective Ce;—

Countries

China

Contacts

Public ContactShen Sun

Obstetrics and Gynecology Hospital of Fudan University, Shanghai, China

sunshen1980@126.com+86 15800391773

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026