Istituto Ortopedico G. Pini
Milan, Milano, 20122, Italy
NCT Number: NCT02384915
The aim of the study is to compare the time of home discharge in day-case patients receiving either a spinal anesthesia or a combined sciatic-femoral nerve block for knee arthroscopy
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Notify Me18 year and older
All sexes
Interventional
Phase 4
Milan, Milano, 20122, Italy
Two groups: the first receive a spinal anesthesia injecting 2% hyperbaric prilocaine 40 mg with the patients in lateral decubitus and the surgical limb declive, the second a combined ultrasound-guided sciatic-femoral nerve block injecting 25 ml of 2% mepivacaine solution.
Onset time, performance time, duration of the block, time of voiding, as well as the time of home discharge will be evaluated.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Other names: prilotekal
Other names: carbocaine
ultrasound-guided 25 ml 2% mepivacaine injection on both femoral and sciatic nerve
intrathecal injection of 40 mg hyperbaric prilocaine
Time frame: 12 hours
ASST Gaetano Pini-CTO
Other
Spinale Unilaterale o Blocco Nervoso Periferico Per le Artroscopie di Ginocchio in Day Surgery. Confronto Prospettico Randomizzato
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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