About this trial
Evaluation of potential nerve damage after radial CAG/PCI.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
The patient must be able to give informed consent
Disqualifiers
Pregnancy
Negative Barbeau test
Trial population
Patients suspected of ischemic heart disease scheduled for radial CAG/PCI at Aarhus University Hospital
Trial design
Cohort
Prospective
Treatments tested in this trial
Not listed
Trial groups
Trial outcomes
Primary outcomes
Neurophysiological measurements
The primary aim is the incidence/presence of electrofysiological signs of median and/or ulnar nerve lesion at the wrist and the presence of carpaltunnel syndrom. The electrodiagnosis of carpaltunnelsyndrom will be determined from the clinical picture and signs of prolonged distal motor lantency and reduced motor and sensory nerveconduction velocity across the wrist and/or reduced amplitudes of the median nerve and normal ulnar nerve at the wrist.
Secondary outcomes
Severity of hand symptoms and hand dysfunction
Boston questionaire
Severity of hand symptoms and hand dysfunction
QuickDash questionaire
Sponsors and contacts
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