Distal radius fracture
Conditions
Interventions
Experimental Group:Performed an ultrasound-guided superficial radial nerve block
anesthetic: 5 mL of 0.33% ropivacaine.
Control group:Performed an ultrasound-guided interscalene brachial plexus block
anesthetic agent: 20 mL of 0.33% ropivacaine
Sponsors
Traditional Chinese Medicine Hospital of Renshou County
Eligibility
Sex/Gender
All
Age
18 Years to 72 Years
Inclusion criteria
Inclusion criteria: 1.All subjects were diagnosed with distal radius fractures based on clinical imaging; 2.All subjects met the indications for closed reduction; 3.No gender restrictions; 4.Age 18–72 years; 5.American Society of Anesthesiologists (ASA) classification grades I–III; 6.Both patients and their families provided informed consent and signed the informed consent form;
Exclusion criteria
Exclusion criteria: 1.Patients with contraindications to nerve blocks (such as infection at the puncture site or allergy to local anesthetics); 2.Pregnant women; 3.Patients who do not understand the procedure, are uncooperative, or have mental disorders; 4.Patients with peripheral neuropathy; 5.Patients with a history of severe cardiovascular, respiratory, renal, or hepatic disease; 6. People who are currently taking anticoagulant medication.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Numerical Rating Scale (NRS) for Post-Block Pain;Onset of block;Duration of analgesia;SPO2; | — |
Secondary
| Measure | Time frame |
|---|---|
| Motion Blocking Time;Blocking operation time;Incidence of Anesthesia-Related Complications; | — |
Countries
China
Contacts
Public ContactQiang Yin
Traditional Chinese Medicine Hospital of Renshou County
Outcome results
None listed