Status:
COMPLETED
Safety/Efficacy Study of Local Anesthetic Prior to Femoral Artery Sheath Removal
Lead Sponsor:
Hamilton Health Sciences Corporation
Conditions:
Syncope, Vasovagal
Pain Intensity
Eligibility:
All Genders
18+ years
Phase:
NA
Brief Summary
This randomized controlled trial will examine the impact of local anesthetic on the frequency of vasovagal reactions and the patients perception of pain during femoral arterial sheath removal after pe...
Detailed Description
Patients undergoing percutaneous coronary intervention(PCI) will be randomized to receive subcutaneous local anesthetic (Lidocaine 2% without epinephrine)or no local prior to removal of femoral arteri...
Eligibility Criteria
Inclusion
- Percutaneous Coronary Intervention
- Femoral arterial sheath
Exclusion
- Less than 18 years old
- Emergency procedure
- Transferred out of heart investigation unit prior to sheath removal
- Radial or brachial sheath
- Closure devise
- Venous sheath insitu
- Intra-aortic balloon pump insitu
- Tranvenous pacing
- Mechanical ventilation
- Cognitive impairment
- Unable to read English
- Lidocaine allergy
Key Trial Info
Start Date :
May 1 2007
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 1 2007
Estimated Enrollment :
78 Patients enrolled
Trial Details
Trial ID
NCT00465439
Start Date
May 1 2007
End Date
September 1 2007
Last Update
August 22 2008
Active Locations (1)
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1
Hamilton Health Science-Heart Investigation Unit
Hamilton, Ontario, Canada, L8N 2S2