Proper Dosage of Ketamine in Intravenous Regional Anesthesia
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ClinicalTrials.gov Identifier: NCT00221871
Recruitment Status : Unknown
Verified September 2005 by University Health Network, Toronto. Recruitment status was: Recruiting
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.
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Layout table for eligibility information
Ages Eligible for Study:
18 Years to 70 Years (Adult, Older Adult)
Sexes Eligible for Study:
Accepts Healthy Volunteers:
Weight: 50-100 kg
ASA: I, II, III
Carpal tunnel syndrome surgery, tenolysis, ganglion removal or any peripheral hand surgery that can be done by IVRA.
Contraindication to IVRA such as sickle cell disease.
Any known hypersensitivity reaction to Ketamine.
History of chronic pain or regular medication with analgesics.