NCT02314650
Completed
Not Applicable
Effect of Transcutaneous Electrical Acupoint Stimulation on Propofol Consumption During General Anesthesia
Air Force Military Medical University, China1 site in 1 country162 target enrollmentAugust 25, 2015
ConditionsAnesthesia
Overview
- Phase
- Not Applicable
- Intervention
- Not specified
- Conditions
- Anesthesia
- Sponsor
- Air Force Military Medical University, China
- Enrollment
- 162
- Locations
- 1
- Primary Endpoint
- propofol consumption
- Status
- Completed
- Last Updated
- 3 years ago
Overview
Brief Summary
The study is aimed at whether transcutaneous electrical acupoint stimulation (TEAS) during general anesthesia could reduce the need for propofol in patients undergoing minor surgery.
Investigators
Zhihong LU
Dr
Air Force Military Medical University, China
Eligibility Criteria
Inclusion Criteria
- •Patients undergoing minor surgeries including laparoscopic surgery and breast surgery under general anesthesia
- •Patients with written informed consent
Exclusion Criteria
- •Patients with difficulty to communicate,including psychiatric disorder and Alzheimer's disease
- •Patients with drug abuse
- •Patients with disease of central nervous system
- •Patients with renal or hepatic dysfunction
Outcomes
Primary Outcomes
propofol consumption
Time Frame: from induction to the end of surgery,at an average of 1 hour
Secondary Outcomes
- effect site concentration of propofol at awake(from end of propofol infusion to open eyes to verbal command,at an average of 30 minutes)
- nausea and vomiting during stay at postanesthesia care unit(30min after surgery)
- time to extubation(from end of propofol infusion to open eyes to verbal command,at an average of 30 minutes)
- time to awake(from end of propofol infusion to open eyes to verbal command,at an average of 30 minutes)
- highest sedation score during stay at postanesthesia care unit(from end of surgery to discharge from post anesthesia care unit, at an average of 1 hour)
Study Sites (1)
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