No target disease
Conditions
Interventions
Dex:reveive Dex sedation
Pro:receive propofol sedation
Sponsors
Beijing Tongren Hospital, Capital Medical University
Eligibility
Sex/Gender
Male
Inclusion criteria
Inclusion criteria: Twenty healthy male subjects(ASA physical status I, right-handed, non-smoking, normal-weight), aged 25–30 years, will be enrolled in this study. All subjects should receive a detailed pre-study examination including an interview, physical status assessment, laboratory testing and a 12-lead ECG. Subjects are not allowed to use alcohol or any medication 48 hours before the study and all fasted at least 8 hours.
Exclusion criteria
Exclusion criteria: Male subjects who have cardiovascular problems,mental disease or severe bradycardia will be exclude from this study.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| the amplitude and latency of AEFP;BIS value;counting ability; | — |
Countries
China
Contacts
Public ContactTianzuo Li
Beijing Shijitan Hospital
Outcome results
None listed