Treatment for Pain

N/A

Waitlist Available

Led By Colin McCartney, MD

Research Sponsored by University Health Network, Toronto

Eligibility Criteria Checklist

Specific guidelines that determine who can or cannot participate in a clinical trial

Must have

Be older than 18 years old

Timeline

Screening 3 weeks

Treatment Varies

Follow Up up to 5 years

Awards & highlights

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.

Timeline

Screening ~ 3 weeks3 visits

Treatment ~ Varies

Follow Up ~ up to 5 years

Screening ~ 3 weeks

Treatment ~ Varies

Follow Up ~up to 5 years

This trial's timeline: 3 weeks for screening, Varies for treatment, and up to 5 years for reporting.

Treatment Details

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Who is running the clinical trial?

University Health Network, TorontoLead Sponsor

1,514 Previous Clinical Trials

500,205 Total Patients Enrolled

6 Trials studying Pain

2,512 Patients Enrolled for Pain

Colin McCartney, MDPrincipal InvestigatorUniversity Health Network, Toronto

2 Previous Clinical Trials

244 Total Patients Enrolled

~16 spots leftby Sep 2025

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