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Clinical Trial Summary

Ketamine added to Lidocaine can increase duration of pain relief following intraveonous regional anesthesia (IVRA). The purpose of this dose response study is to determine the minimum effective dosage of intravenous Ketamine, added to 3 mg/kg of Lidocaine. We anticipate that one dosage will provide us with the proper balance between sufficient anesthesia and minimal side effects.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Intervention Model: Parallel Assignment, Masking: Single Blind, Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00221871
Study type Interventional
Source University Health Network, Toronto
Contact Colin McCartney, MD
Phone (416)603-5118
Email colin.mccartney@uhn.on.ca
Status Recruiting
Phase N/A
Start date January 2004
Completion date January 2005

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