Analgesic effect of Nefopam hydrocholoride after arthroscopic rotator cuff repair
Not Applicable
Completed
- Conditions
- Not Applicable
- Registration Number
- KCT0002325
- Lead Sponsor
- The Catholic University of Korea, Seoul St. Mary's Hospital
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Completed
- Sex
- All
- Target Recruitment
- 140
Inclusion Criteria
Adults patients who have rotator cuff tear or inflammation. (Reference from Orthopedic diagnosis criteria)
- C2 (moderate tear < 2cm of only one tendon without retraction) in Southern California
Orthopedic Institute rotator cuff classification system
- no accompanied with complex tear related to rotator cuff
Exclusion Criteria
less than 19year old, older than 71year
Seizure or seizure history
severe hepatic, renal, cerebral disease
severe cardiovascular disease including MI(myocardiac infarction)
administration of Monoamine Oxidase inhibitor
closed - angle glaucoma (elevated ocular pressure)
patients with hypersensitivity to this drug component
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method preemptive analgesic effect of preoperative administration of nefopam
- Secondary Outcome Measures
Name Time Method Postoperative preventive analgesic effect of nefopam hydrochloride in time sequence regardless of nerve block