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Escitalopram as a Treatment for Pain in Polyneuropathy

Escitalopram as a Treatment for Pain in Polyneuropathy. A Double-Blind, Randomized, Placebo Controlled Trial.

Status
Completed
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00162968
Enrollment
50
Registered
2005-09-13
Start date
2004-12-31
Completion date
2007-04-30
Last updated
2007-04-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Pain, Polyneuropathies

Keywords

polyneuropathies, pain, drug effects, escitalopram, serotonin uptake inhibitors

Brief summary

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.

Detailed description

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.

Interventions

DRUGescitalopram

Sponsors

Aarhus University Hospital
CollaboratorOTHER
H. Lundbeck A/S
CollaboratorINDUSTRY
Odense University Hospital
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
20 Years to 80 Years
Healthy volunteers
No

Inclusion criteria

* median total pain score at baseline week \>=4 on a 10 point numerical rating scale * characteristic symptoms of polyneuropathy within at least 6 months * diagnosis confirmed by physical examination, neurophysiologic exam. and/or quantitative sensory testing * pain at least 4 of 7 days * fertile women are using anticonceptive

Exclusion criteria

* other cause to pain than polyneuropathy * former allergic reactions on escitalopram * known adverse events on escitalopram * pregnancy or nursing * critical disease (terminal cancer, cardial incompensation or critical renal or lung disease) * treatment with monoamine oxidase inhibitors between the trial or 2 weeks before or after treatment with other antidepressants, antiepileptic agents or opioids

Design outcomes

Primary

MeasureTime frame
pain relief

Secondary

MeasureTime frame
effect on total pain and different subtypes of pain
effect on quantitative sensory testing
effect on pain related sleep disturbances
effect on quality of life
to determine if depression before treatment predicts an eventual pain relieving effect of escitalopram

Countries

Denmark

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026