drugset / Trial / NCT01452880

Remifentanil in Extracorporeal Shock Wave Lithotripsy

NCT01452880

Phase 4 Completed 228 enrolled University of Roma La Sapienza
RandomizedParallel-groupDouble-blindTreatment

Summary

The purpose of this study is to compare the analgesic efficacy and side effects induced by administration of two different infusion rates of remifentanil, 0,05 mcg/ Kg/ min versus 0,1mcg/ Kg/ min, in order to determine which one is the most appropriate analgesic treatment to face extracorporeal shock wave lithotripsy.

Timeline

Start
2010-01
Primary completion
2010-07
Completion
2010-07

Drugs

EvaluationDrugModalityDoseRoute
Subject Remifentanil Small molecule 0.05 ug/kg Intravenous
Subject Remifentanil Small molecule 0.1 ug/kg Intravenous

Indications