The Efficacy and Safety of Chloroprocaine 1% and 2% in Pediatric Population
Status:
Recruiting
Trial end date:
2021-12-31
Target enrollment:
Participant gender:
Summary
Randomized, multi-center, double-blind, two-armed, parallel active groups, prospective trial
to evaluate the efficacy and safety of local anesthetic Chloroprocaine at two different
concentrations ( at 1% and 2%) in a pediatric population subjected to peripheral nerve block
due to Inguinal hernia repair or Flat foot surgery. The present Protocol is part of an
extensive Pediatric Investigational Plan (PIP) in the contest of the marketing authorization
application of chloroprocaine use for perineural block. The PDCO has adopted a positive
opinion.