Comparison of propofol, dexamedetomidine and their combination’s effect for sedatio
Not Applicable
Recruiting
- Conditions
- Not Applicable
- Registration Number
- KCT0001284
- Lead Sponsor
- Hanyang University Seoul Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 90
Inclusion Criteria
patients who reqiure Brachial plexus block.
American Society of Anesthesiologists’ classification from 1 to 3.
Exclusion Criteria
patients whe do not agree with the experiment.
Patients with impaired cognitive function.
Patients with serious neurological, cardiac, liver, and kidney disease.
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method the extent of loss of airway patent;The change of the blood pressure
- Secondary Outcome Measures
Name Time Method bispectral index ;observer assessment of alertness/sedation (OAA/S) score;Heart rate ;oxygen saturation;end tidal carbon dioxide;respiratory rate ;hypoxia, spontaneous movement, cough, nausea, vomiting, agitation;Onset time of designated level of sedation and recovery time;satisfaction level and recall, nausea, vomiting