NCT01981369View on ClinicalTrials.gov

Effect of Intravenous Dexmedetomidine on Analgesic Duration of Infraclavicular Block

NACompletedINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

January 31, 2014

Primary Completion Date

July 31, 2016

Study Completion Date

December 31, 2016

Conditions
Postoperative Pain
Interventions
DRUG

Dexmedetomidine

Intravenous sedation with dexmedetomidine

DRUG

Propofol

Intravenous sedation with propofol

PROCEDURE

Infraclavicular block

All patients will receive ultrasound guided infraclavicular block with the standard protocol of the Block Room in St. Joseph Hospital.

Trial Locations (1)

N6A 4V2

Saint Joseph's Health Care London, London

All Listed Sponsors
lead

London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's

OTHER

NCT01981369 - Effect of Intravenous Dexmedetomidine on Analgesic Duration of Infraclavicular Block | Biotech Hunter | Biotech Hunter