drugset / Trial / NCT00815893

The Feasibility of Dexmedetomidine for Awake Fiberoptic Nasal Intubation

NCT00815893

RandomizedSingle-groupQuadruple-blindTreatment

Summary

The objective of this study is to evaluate the feasibility of dexmedetomidine infusion for oral cancer patients undergoing awake fiberoptic nasal intubation. We hypothesized that a loading dose of intravenous dexmedetomidine before awake fiberoptic nasal intubation for oral cancer patients undergoing general anesthesia will provide adequate sedation and analgesia without respiratory depression and upper airway obstruction.

Timeline

Start
2008-08
Primary completion
2009-08
Completion
2009-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Dexmedetomidine Other / unclassified 1 ug/kg Intravenous
Comparator Propofol Small molecule 3 ug/ml

Indications

No indication recorded.