drugset / Trial / NCT01452880
Remifentanil in Extracorporeal Shock Wave Lithotripsy
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
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | Remifentanil | Small molecule | 0.05 ug/kg | Intravenous |
| Subject | Remifentanil | Small molecule | 0.1 ug/kg | Intravenous |