The Effects of Different Doses of Dexmedetomidine on Propofol Requirement for Loss of Consciousness Undergoing Bispectral Index: a Double-blinded, Placebo-controlled Trial

• Status: Completed
• Trial end date: 2016-08-01
• Target enrollment: 0
• Participant gender: All

Summary

The purpose of this study is to evaluate the effects of different dexmedetomidine on the propofol requirement for loss of consciousness undergoing bispectral index.

• Phase: N/A
• Accepts Healthy Volunteers?: No

Details

• Lead Sponsor: General Hospital of Ningxia Medical University
• Treatments: Dexmedetomidine; Propofol

Criteria

Inclusion Criteria:

• ASA physical status I-II

• Aged 18-65 years

• Body Mass Index 18.0～24.5 kg/m2

• Without hearing impairment

Exclusion Criteria:

• Bradycardia

• Atrioventricular block

• Neurologic disorder and recent use of psychoactive medication

• Allergic to the drugs