Preventive effect of maxijesic on rebound pai
- Conditions
- Diseases of the musculoskeletal system and connective tissue
- Registration Number
- KCT0009479
- Lead Sponsor
- Samsung Medical Center
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 78
Adults between 19 and 70 years of age
- Patients undergoing bone surgery of the hand or wrist with supraclavicular block
- American Society of Anesthesiologists Physical Status I, II, III
- Pregnant, lactating women
- Patients with serious coagulopathy (INR 1.5 or higher on the last blood coagulation test before surgery)
- Patients with unstable coronary artery disease, congestive heart failure, arrhythmia, and myocarditis
- Patients with cerebrovascular disease
- Patients with systemic infection or current infection in the area where supraclavicular block surgery will be performed (above the clavicle)
- Patients who did not understand this study and expressed their intention not to participate in the study
- Patients allergic to local anesthetics
- Patients contraindicated in the test drug (Maxijesic Injection)
? Patients with a history of hypersensitivity to study drug or its components
? Patients with active alcoholism
? Patients with gastrointestinal ulcers, gastrointestinal bleeding, or patients with a history of gastrointestinal ulcers or gastrointestinal bleeding
? Patients with severe blood abnormalities
? Patients with severe liver and kidney disorders
? Patients with severe cardiac dysfunction
? Patients with severe hypertension
? Patients with bronchial asthma or a history of it
? Patients who have or have a history of hypersensitivity, such as an allergic reaction, to aspirin or other non-steroidal anti-inflammatory drugs.
? Patients experiencing pain before and after coronary artery bypass surgery
? Pregnant women
? Patients taking the following drugs: barbiturates, tricyclic antidepressants
? Patients receiving high-dose methotrexate for anticancer therapy
- Others: autoimmune disease, history of drug hypersensitivity reaction, food allergy, chronic hives
- Patients with a serious psychiatric history that may affect patient evaluation
- Patients who failed supraclavicular block surgery
Study & Design
- Study Type
- Interventional Study
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method Rebound pain score
- Secondary Outcome Measures
Name Time Method pain scores;Worst pain ;The time of first analgesic request;opioid consumption;Patient satisfaction: analgesia ,fist nigh sleep;Adverse event: nausea and vomiting ,dizziness, respiratory depression, block related complication