Clinical Trial Center
Zurich, Switzerland
NCT Number: NCT00900913
The purpose of this study is to compare the effect of intravenous ropivacaine and lidocaine on the receptive field of primary sensory afferents and their influence on the vascular bed.
*Trial with medicinal product
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Notify Me18 year–65 year
Male
Interventional
Phase 4
Zurich, Switzerland
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
intravenous infusion 1 mg/kg bw
Other names: Naropin
Time frame: 1 year
University of Zurich
Other
Effect of Systemic Ropivacaine on Hyperalgesia, Flare Reaction and Peripheral
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