This clinical trial is focused on studying the treatment of distal radius fractures, which are breaks near the wrist end of the forearm bone. The trial will compare two methods for managing these fractures: a brachial plexus nerve block and standard care. A brachial plexus nerve block is a procedure where a numbing medication is injected near the nerves of the shoulder to block pain in the arm. The medication used in this procedure is a combination of epinephrine and lidocaine hydrochloride, which is administered as a solution for injection.
The purpose of the study is to evaluate the effects of using an ultrasound-guided brachial plexus nerve block for patients who need a closed reduction, which is a non-surgical method to realign the broken bone. Participants in the study will receive either the nerve block or standard care, and their progress will be monitored over a period of time. The study will look at various outcomes, such as the need for surgery within 90 days, any complications related to the treatment, and the level of pain experienced during the procedure.
Throughout the study, researchers will also assess the position of the fracture after the procedure and any new injuries or complications that may arise. The trial aims to provide valuable information on the benefits and risks of using a brachial plexus nerve block compared to standard care for treating distal radius fractures.
Denmark 
