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| Sponsor: | Odense University Hospital |
|---|---|
| Collaborators: |
Aarhus University Hospital H. Lundbeck A/S |
| Information provided by: | Odense University Hospital |
| ClinicalTrials.gov Identifier: | NCT00162968 |
Purpose
Many people with polyneuropathy suffer from pain which is difficult to treat. Escitalopram is a relatively new drug used in the treatment of depression. Escitalopram’s action mechanism on the brain suggests that escitalopram also may have an effect on neuropathic pain. This study will test the efficacy of escitalopram in patients with painful polyneuropathy.
| Condition | Intervention | Phase |
|---|---|---|
|
Pain Polyneuropathies |
Drug: escitalopram |
Phase IV |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Efficacy Study Intervention Model: Crossover Assignment Masking: Double-Blind Primary Purpose: Treatment |
| Official Title: | Escitalopram as a Treatment for Pain in Polyneuropathy. A Double-Blind, Randomized, Placebo Controlled Trial. |
| Estimated Enrollment: | 50 |
| Study Start Date: | December 2004 |
| Study Completion Date: | April 2007 |
Tricyclic antidepressants appear to be the most efficacious treatment of painful polyneuropathy. However, these drugs are contraindicated in some patients and a substantial number of patients decline treatment due to side-effects. Therefore, effective drugs that are better tolerated are needed. Clinical and basic research has demonstrated that drugs with serotonergic action can alleviate neuropathic pain. Escitalopram increases serotonin concentration in the central nervous system, suggesting that it might be a potential alternative to current treatments of neuropathic pain. The aim of this study is to test if escitalopram would relieve painful polyneuropathy.
Comparisons: Treatment with 20 mg escitalopram daily will be compared in a cross-over design with placebo. Each treatment period will last 6 weeks. During the last week of each treatment period, the dose will be tapered.
Eligibility| Ages Eligible for Study: | 20 Years to 80 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Denmark | |
| Danish Pain Research Center, Aarhus University Hospital, Noerrebrogade 44 | |
| Aarhus, Denmark, 8000 | |
| Dept. of Neurology, Odense University Hospital, Sdr. Boulevard 29 | |
| Odense, Denmark, 5000 | |
| Principal Investigator: | Soeren H Sindrup, MD, PhD | Odense University Hospital, Dept. of neurology |
More Information
| ClinicalTrials.gov Identifier: | NCT00162968 History of Changes |
| Other Study ID Numbers: | escit01 |
| Study First Received: | September 9, 2005 |
| Last Updated: | April 23, 2007 |
| Health Authority: | Denmark: Danish Medicines Agency |
|
polyneuropathies pain drug effects escitalopram serotonin uptake inhibitors |
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Polyneuropathies Peripheral Nervous System Diseases Neuromuscular Diseases Nervous System Diseases Dexetimide Citalopram Serotonin Uptake Inhibitors Antiparkinson Agents Anti-Dyskinesia Agents Central Nervous System Agents Therapeutic Uses Pharmacologic Actions Parasympatholytics |
Autonomic Agents Peripheral Nervous System Agents Physiological Effects of Drugs Muscarinic Antagonists Cholinergic Antagonists Cholinergic Agents Neurotransmitter Agents Molecular Mechanisms of Pharmacological Action Antidepressive Agents, Second-Generation Antidepressive Agents Psychotropic Drugs Neurotransmitter Uptake Inhibitors Serotonin Agents |