Ultrasound-guided Block of the Supraclavicular Nerves in Clavicular Fractures (US-SCNB_Clav)
Clavicular Fracture, Pain, Acute
About this trial
This is an interventional treatment trial for Clavicular Fracture focused on measuring ultrasound-guided regional anesthesia, Clavicular fracture, Emergency Department, pain management
Eligibility Criteria
Inclusion Criteria:
- adult ED-patients with sonographic and / or radiologically diagnosed clavicular fracture, who are scheduled for operation within the next 24 hours
- older then 18 years
- no known allergies to local anesthetic drugs
Exclusion Criteria:
- refusal of the procedure by the patient
- infection at the site of possible injection of local anaesthetics
- known allergies against local anaesthetics
- inability of consent or no carer
Sites / Locations
- Merian Iselin Klinik
Arms of the Study
Arm 1
Arm 2
Active Comparator
Active Comparator
Group 1: Control
Group 2: Nerve Block
Systemic conventional pain management. Adult patients with acute fractures of the clavicle, who are scheduled to have internal fixation of the fracture within the next 24 hours receive oral and intravenous pain management.
Adult patients with acute fractures of the clavicle, who are scheduled for an internal fixation of the fracture within the next 24 hours will receive an ultrasound-guided block of the supraclavicular nerves using a maximum of 3 ml of a long-acting local anesthetic. The injection is carried out directly in the emergency department following a sonographic or radiological diagnosis.