Clinical trial
Safety/Efficacy Study of Local Anesthetic Prior to Femoral Artery Sheath Removal
NCT00465439 · Hamilton Health Sciences Corporation, Other · Completed
Key facts
| NCT number | NCT00465439 |
|---|---|
| Title | Safety/Efficacy Study of Local Anesthetic Prior to Femoral Artery Sheath Removal |
| Official title | Randomized Controlled Trial Examining the Effect of Subcutaneous Xylocaine 2% on the Incidence of Vasovagal Reactions and Pain Intensity During Femoral Artery Sheath Removal. |
| Lead sponsor | Hamilton Health Sciences Corporation, Other |
| Status | Completed |
| Study type | Interventional |
| Conditions | Syncope, Vasovagal, Pain Intensity |
| Intervention type | Drug |
| Interventions | Subcutaneous Lidocaine 2% (Xylocaine) without epinephrine |
| Enrollment | 78 |
| Start date | May 1, 2007 |
| Primary completion | Sep 1, 2007 |
| Completion | Sep 1, 2007 |
| First posted | Apr 25, 2007 |
| Last update posted | Aug 22, 2008 |
| Countries | Canada |
At a glance
- 1–9 Study sites
- No Results posted
- None Linked FDA submissions
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date: