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

NCT00465439 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 78

Last updated 2008-08-22

No results posted yet for this study

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 percutaneous coronary intervention.

Conditions

  • Syncope, Vasovagal
  • Pain Intensity

Interventions

DRUG

Subcutaneous Lidocaine 2% (Xylocaine) without epinephrine

10 ml subcutaneously

Sponsors & Collaborators

  • Hamilton Health Sciences Corporation

    lead OTHER

Principal Investigators

  • Allison Cook, BScN · Hamilton Health Science

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2007-05-31
Primary Completion
2007-09-30
Completion
2007-09-30

Countries

  • Canada

Study Locations

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Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00465439 on ClinicalTrials.gov