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

> **NCT00465439** · NA · COMPLETED · sponsor: **Hamilton Health Sciences Corporation** · enrollment: 78 (actual)

## Conditions studied

- Syncope, Vasovagal
- Pain Intensity

## Interventions

- **DRUG:** Subcutaneous Lidocaine 2% (Xylocaine) without epinephrine

## Key facts

- **NCT ID:** NCT00465439
- **Lead sponsor:** Hamilton Health Sciences Corporation
- **Sponsor class:** OTHER
- **Phase:** NA
- **Study type:** INTERVENTIONAL
- **Status:** COMPLETED
- **Start date:** 2007-05
- **Primary completion:** 2007-09
- **Final completion:** 2007-09
- **Target enrollment:** 78 (ACTUAL)
- **Last updated:** 2008-08-22


## Primary source

ClinicalTrials.gov registry: https://clinicaltrials.gov/study/NCT00465439

## Citation

> US National Library of Medicine, ClinicalTrials.gov registration NCT00465439, "Safety/Efficacy Study of Local Anesthetic Prior to Femoral Artery Sheath Removal". Retrieved via AI Analytics 2026-09-17 from https://api.ai-analytics.org/clinical/NCT00465439. Licensed CC0.

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