The goal of this study is to compare the analgesic effect of a blind fascia iliaca compartment block to an ultrasound-guided femoral nerve block in patients that present to the emergency department with hip fractures.
Hip fractures often present to the emergency department and elderly, already fragile, patients are overrepresented. The pain associated with a hip fracture can be severe and have deleterious effects on the patient. Many studies, and a Cochrane review, have shown that a peripheral nerve block provides good pain relief and has many benefits compared to traditional pain relief, such as intravenous morphine. There is less consensus regarding which kind of nerve block, and which technique, is best to use. Many studies compared different kinds of nerve blocks to traditional methods, or more recently compared different kinds of ultrasound-guided techniques to each other. This study proposes to compare the widely used technique of a blind fascia iliaca compartment block (FICB) to an ultrasound-guided femoral nerve block (FNB) that is currently being rolled out locally as an alternative. During the implementation period of this new clinical routine, it will be possible to compare the efficacy of FICB and FNB in reducing participant-reported pain.
Study Type
OBSERVATIONAL
Enrollment
100
Blind technique.
Ultrasound guided.
Ropivacaine dosed according to local guidelines.
Akutmottagningen US Östergötland
Linköping, Östergötland County, Sweden
RECRUITINGMean Change from Baseline in Pain Scores on the Numeric Rating Scale (0 to 10, where 10 is Maximum Pain) at 30 minutes after Administration of Block, at Rest and During Active Hip Flexion
Change in reported pain score should be at least one whole unit on the numeric rating scale.
Time frame: Measured 30 minutes after administered nerve block.
Ratio of Failed Blocks
Defined by a failure to reduce reported pain 30 minutes after administered block by at least one whole unit on the numeric rating scale
Time frame: Through study completion, an average of 1 year
Rate of Complications
Comparing the rate of any reported complication between cohorts
Time frame: Through study completion, an average of 1 year
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