Concentration-Volume Relationship in Infraclavicular Block
Status:
Completed
Trial end date:
2016-10-01
Target enrollment:
Participant gender:
Summary
This prospective, randomized, double blind study aims to determine the optimal volume for
adequate sensorial and motor blockade following an infraclavicular block. Patients will be
randomized into three groups. Using a constant dose of local anesthetics (45mg bupivacaine
180mg prilocaine), different volumes will be used in each of the groups (First group; 18mL,
second group; 27mL, third group; 36mL). Onset, duration and quality of sensory and motor
block will be compared for patients between groups