drugset / Trial / NCT05958589

Caudal Block for Inguinal Hernioplasty in Children

NCT05958589

Phase 3 Completed 70 enrolled University of Novi Sad
RandomizedParallel-groupSingle-blindTreatment

Summary

This is a prospective, randomized, controlled clinical study designed to determine the effectiveness of caudal block combined with general anesthesia in providing intra- and postoperative analgesia, and its effect on hemodynamic stability and drug consumption.

Timeline

Start
2022-01-08
Primary completion
2024-07-20
Completion
2024-07-20

Drugs

EvaluationDrugModalityDoseRoute
Subject Levobupivacaine Other / unclassified 0.25 % Other
Subject Levobupivacaine Other / unclassified 2.5 mg/kg Other
Background Fentanyl Other / unclassified 1 ug/kg Intravenous
Background Fentanyl Other / unclassified 1.5 ug/kg Intravenous
Background Midazolam Small molecule 0.5 mg/kg Oral
Background Propofol Small molecule 2 mg/kg Intravenous
Background Propofol Small molecule 3 mg/kg Intravenous
Background Rocuronium Other / unclassified 0.6 mg/kg Intravenous
Background Rocuronium Other / unclassified 1 mg/kg Intravenous

Indications

No indication recorded.