drugset / Trial / NCT01001429

Dexmedetomidine Versus Propofol in Vitreoretinal Surgery

NCT01001429 ↗

Phase 4 Completed 78 enrolled Rutgers, The State University of New Jersey
RandomizedParallel-groupTriple-blindTreatment

Summary

The investigators would like to determine if using Dexmedetomidine alone or in a reduced dose can prevent or reduce the incidence of adverse effects, while providing adequate sedation, and respiratory stability as compared to propofol.

Timeline

Start
2009-10
Primary completion
2013-03
Completion
2013-11

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexmedetomidine Other / unclassified 0.2 ug/kg Intravenous
Subject Dexmedetomidine Other / unclassified 0.7 ug/kg Intravenous
Comparator Propofol Small molecule 25 ug/kg Intravenous
Comparator Propofol Small molecule 100 ug/kg Intravenous

Indications