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Plasma Concentration of Ketamine and Norketamine .

CompletedNot applicableNCT02016664
View the official record on ClinicalTrials.gov

Recruiting status changes often. Contact the study team listed on ClinicalTrials.gov, and talk to your doctor before joining a study.

Brief summary (from the registry)

Oral ketamine is increasingly used by doctors to both reduce the amount of narcotic pain medication consumed and to improve chronic pain management in difficult cases. How much is absorbed when taken orally, as opposed to intravenously ,is unknown. Ketamine may cause sedation, and occasionally cognitive impairment. Therefore, there are safety concerns associated with its usage as an out-patient may engage in activities where cognitive impairment is dangerous,such as driving. This study is designed to measure the plasma concentrations of ketamine and its active metabolite, norketamine, in people taking low dose oral ketamine for chronic pain. The goal of the study is to verify that low dose oral ketamine produces plasma concentrations below the level associated with toxic symptoms,and thus can be safely used long-term for the treatment of chronic pain .

Study details

Official title
Plasma Concentration of Ketamine and Norketamine in Patients on Oral Ketamine for Chronic Neuropathic Pain : A Pilot Study.
Conditions
Interventions
Sponsor
London Health Sciences Centre Research Institute OR Lawson Research Institute of St. Joseph's
Start date
2014-04
Primary completion
2015-12
Sex
All
Age range
from 18 Years to 75 Years
Results posted
No results posted in this snapshot
Countries
Canada
Total sites listed
1

Eligibility criteria

Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * Patient currently takes oral ketamine for the treatment of chronic neuropathic pain. * Age \>18 and \< 75 years * Both males and females 4.Ability to speak English adequately to understand the consent and participate in the study * No other route of ketamine within past 7 days (Topical/IV) Exclusion Criteria: * Patient receiving liver enzyme inducers or inhibitors of Cytochrome CYP3A4, or CYP2B6 like clarithromycin, rifampin, and recent ingestion of grapefruit juice. * Patients who have had gastric bypass surgery * Patients who did not follow the prescribed protocol * Renal Failure defined as Creatinine Clearance \<50 mL/min * Hepatic insufficiency by history

Canadian sites (1)

FacilityCityProvince
St.Joseph's Health Care, Western UniversityLondonOntario

Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT02016664