NCT00465439View on ClinicalTrials.gov

Safety/Efficacy Study of Local Anesthetic Prior to Femoral Artery Sheath Removal

NACompletedINTERVENTIONAL
Enrollment

78

Participants

Timeline

Start Date

May 31, 2007

Primary Completion Date

September 30, 2007

Study Completion Date

September 30, 2007

Conditions
Syncope, VasovagalPain Intensity
Interventions
DRUG

Subcutaneous Lidocaine 2% (Xylocaine) without epinephrine

10 ml subcutaneously

Trial Locations (1)

L8N 2S2

Hamilton Health Science-Heart Investigation Unit, Hamilton

All Listed Sponsors
lead

Hamilton Health Sciences Corporation

OTHER

NCT00465439 - Safety/Efficacy Study of Local Anesthetic Prior to Femoral Artery Sheath Removal | Biotech Hunter | Biotech Hunter