Reducing pain of microemulsion propofol injection: a double blind randomized study of three methods of tourniquet and lidocaine
Not Applicable
- Conditions
- elective surgery
- Registration Number
- JPRN-UMIN000010725
- Lead Sponsor
- Korea University
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Complete: follow-up complete
- Sex
- All
- Target Recruitment
- 140
Inclusion Criteria
Not provided
Exclusion Criteria
patints with known hypersensitivity to lidocaine or microemulsion propofol, impaired communication, a renal, hepatic, cardiac, or neurologic problem, or a hypovolemic state and those who refused to provide informed consent were excluded.
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Reduce the incidence and intensity of microemulsion propofol injection pain
- Secondary Outcome Measures
Name Time Method