The Effective Effect-Site Propofol Concentration for Induction and Intubation for Schnider Model in Parturients

• Status: Unknown status
• Trial end date: 2017-12-01
• Target enrollment: 0
• Participant gender: Female

Summary

The aim of this study was to determine the target propofol concentration needed to provide adequate hypnosis for induction and tracheal intubation for Schnider model using total body weight (TBW) in parturients. In addition, investigators wanted to define the hemodynamic adverse effects associated with these propofol target concentrations.

• Phase: N/A
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Fudan University
• Treatments: Propofol

Criteria

Inclusion Criteria:

• Thirty-six women undergoing elective cesarean section under general anesthesia were enrolled in this prospective observational study.

Exclusion Criteria:

• Diabetes controlled by insulin

• Preeclampsia

• Heart diseases

• History of taking drugs potentially affecting cardiovascular system.

• Patients fasted for at least 8 hours before surgery and no premedication was given