None listed
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: - 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
Exclusion criteria
Exclusion criteria: - 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
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Rebound pain score | — |
Secondary
| Measure | Time frame |
|---|---|
| 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 | — |
Countries
Korea, Republic of
Contacts
Samsung Medical Center