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• W2015365870 abstract "The N-methyl-d-aspartate receptor plays an important role in central sensitization of neuropathic pain and N-methyl-d-aspartate receptor antagonists, such as ketamine, memantine and dextromethorphan may be used for persistent pain. However, ketamine cannot be repeated too often because of its adverse events. A drug relay would be helpful in the outpatient to postpone or even cancel the next ketamine infusion. This clinical trial evaluates if memantine and/or dextromethorphan given as a relay to ketamine responders may maintain or induce a decrease of pain intensity and have a beneficial impact on cognition and quality of life. This trial is a multi-center, randomized, controlled and single-blind clinical study (NCT01602185). It includes 60 ketamine responder patients suffering from neuropathic pain. They are randomly allocated to memantine, dextromethorphan or placebo. After ketamine infusion, 60 patients received either memantine (maximal dose 20 mg/day), or dextromethorphan (maximal dose 90 mg/day), or placebo for 12 weeks. The primary endpoint is pain measured on a (0–10) Numeric Rating Scale 1 month after inclusion. Secondary outcomes include assessment of neuropathic pain, sleep, quality of life, anxiety/depression and cognitive function at 2 and 3 months. Data analysis is performed using mixed models and the tests are two-sided, with a type I error set at α = 0.05. This study will explore if oral memantine and/or dextromethorphan may be a beneficial relay in ketamine responders and may diminish ketamine infusion frequency. Preservation of cognitive function and quality of life is also a central issue that will be analyzed in these vulnerable patients." @default.
• W2015365870 created "2016-06-24" @default.
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• W2015365870 date "2014-07-01" @default.
• W2015365870 modified "2023-09-24" @default.
• W2015365870 title "Rationale and design of a multicenter randomized clinical trial with memantine and dextromethorphan in ketamine-responder patients" @default.
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• W2015365870 doi "https://doi.org/10.1016/j.cct.2014.06.004" @default.
• W2015365870 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/24948402" @default.
• W2015365870 hasPublicationYear "2014" @default.
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