NCT00864682View on ClinicalTrials.gov

Preventing Propofol-associated Injection Pain

PHASE4CompletedINTERVENTIONAL
Enrollment

156

Participants

Timeline

Start Date

January 31, 2008

Primary Completion Date

March 31, 2009

Study Completion Date

April 30, 2009

Conditions
Pain
Interventions
DRUG

Saline

3.3 mL normal saline

DRUG

Lidocaine / propofol admixture

lidocaine 50 mg plus propofol 50 mg intravenous (iv)

DRUG

lidocaine pretreatment

lidocaine 50 mg iv under tourniquet-control

Trial Locations (1)

98101

Benaroya Research Institute, Seattle

Sponsors
All Listed Sponsors
lead

Benaroya Research Institute

OTHER