postoperative pain in patiets undergoing shoulder arthroscopic surgery
Conditions
Interventions
Control group:0.5% bupivacaine plus dexamethasone with brachial plexus superior trunk block
Observation group:0.31% liposomal bupivacaine with brachial plexus superior trunk block
Sponsors
Zhuji People's Hospital
Eligibility
Sex/Gender
All
Age
18 Years to 70 Years
Inclusion criteria
Inclusion criteria: 1. Patients scheduled for shoulder arthroscopy; 2. ASA I-II; Age 18-70; BMI: 18.5-30 kg/m^2;
Exclusion criteria
Exclusion criteria: 1. The subject refused to participate in the study; 2. history of allergy to local anesthetics; 3. pregnant; 4. Mental nervous system, craniocerebral injury and other diseases lead to inability to communicate and cooperate; 5. Brachial plexus injury; 6. infection, breakage of the puncture of the skin; 7. Coagulation dysfunction;
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Duration of postoperative analgesia; | — |
Secondary
| Measure | Time frame |
|---|---|
| The influence on the muscle strength of the blocked upper limb.;Rehabilitation of shoulder joint function after surgery: Constant-Murley Shoulder Joint Function Score;Hospitalization days;Pain assessment after block;Drug cost;Anesthesia related expenses;Complications: The occurrence of complications such as Horner syndrome, hoarseness, nausea and vomiting was recorded.;Total hospitalization cost;Measurement of unilateral septal muscle mobility;Use of rescue analgesics within 48 hours;Treatment costs related to complications (such as nausea and vomiting); | — |
Countries
China
Contacts
Public ContactXuan Hongmei
Zhuji People's Hospital
Outcome results
None listed