drugset / Trial / NCT02820688

Concentration-Volume Relationship in Infraclavicular Block

NCT02820688

Phase 4 Completed 81 enrolled Bozyaka Training and Research Hospital
RandomizedParallel-groupQuadruple-blindTreatment

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

Timeline

Start
2016-06
Primary completion
2016-10
Completion
2016-10

Drugs

EvaluationDrugModalityDoseRoute
Comparator Bupivacaine Other / unclassified 45 mg
Comparator prilocaine Small molecule 180 mg

Indications

No indication recorded.