Phase
Condition
N/ATreatment
Ropivacaine concentration low
Ropivacaine concentration high
Clinical Study ID
Ages 18-80 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
Patients with distal radius fracture, scheduled for volar plate surgery
Surgery up to 20 days after fracture trauma
18 to 80 years old (inclusive)
ASA 1, 2 or stable ASA 3
Body Mass Index (BMI) 18 to 40 kg/m2 (inclusive)
Weight of 50 kg or more
Ability to communicate sufficiently in a scandinavian language
Capable of giving a signed informed consent
Ability and willingness to understand og be compliant to the study
Exclusion
Exclusion Criteria:
Contemporaneous painful injuries
Existing long-term pain
Peripheral nerve damage in the arm with radius fracture
Patients who prior to fracture trauma use opioids, psycothropic drugs or medication,with or without prescription, with significantly sedative effect on regular basis.
Excessive use of alcohol (more than 15 units of alchol per week for men, more than 8units of alchol per week for women, or patients reporting to be incapable ofavoiding alcohol as long as they use strong opioids).
Progressive neurologic disease (inclusive diabetic neuropathy).
Skin infection at the site for brachial plexus nerve block
Other contraindications for brachial plexus nerve block
Contraindications for ropivacaine, paracetamol, etoricoxib, dexamehtasone oroxycodone
Previous allergic reaction to local anaesthetics or etoricoxib, dexamethasone,oxycodone or paracetamol.
Pregnant or breast-feeding women at surgery day (they do not get excluded if theybecome pregnant in the follow up period after intervention and surgery)
Study Design
Connect with a study center
Oslo University Hospital
Oslo,
NorwayActive - Recruiting

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