prospective trial to validate of efficacy of brachial plexus block duration in patients undergoing orthopedic upper arm surgery when patients are sadated by dexmedetomidine
Not Applicable
Completed
- Conditions
- Diseases of the musculo-skeletal system and connective tissue
- Registration Number
- KCT0002138
- Lead Sponsor
- Chungnam National University Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 102
Inclusion Criteria
americal society of anesthesiologist physical status I-III , aged 20yrs~70yrs
open reduction internal fixation (ORIF) for fractures of the radius or ulnar shortening surgery for ulnar impaction
written informed consent
Exclusion Criteria
Refuse Brachial plexus block
local infection, amide anesthetics(ropivacaine) hypersensitivity
Hypersensitivity or allergy of dexmedetomidine
Neuropathy
Uncontrolled diabetes mellitus
Significant pulmonary disease
Significant cardiovascular disease
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method First analgesic requirement
- Secondary Outcome Measures
Name Time Method First analgesic requirement ??? VAS( visual analog scales);used opioid total dose;vital sign (blood pressure, heart rate) , mRSS