Assessment of the Effectiveness of Ethosuximide in the Treatment of Peripheral Neuropathic Pain.

NCT02100046 — Phase 2, Completed, 114 participants, University Hospital, Clermont-Ferrand

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RegistryNCT02100046, acronym EDONOT
StatusCompleted
PhasePhase 2
Study typeInterventional; randomized, parallel, masking: double, treatment
Enrollment114 (Actual)
SponsorUniversity Hospital, Clermont-Ferrand (Other); collaborators: Fondation Apicil
ConditionsNeuropathic Traumatic Pain, Pain NRS ≥ 4, Peripheral Neuropathic Pain, Neuropathic Pain Diagnostic Questionnaire (DN4) ≥ 4
InterventionsZarontin® (ethosuximide) and Stodal® (Drug)
Datesstart 2014-03-01, primary completion 2016-09-01, completion 2017-01-01, first posted 2014-03-31, last updated 2026-04-21
Locations1 site in France

Related Papers Related Patents Related Grants Related Experts
All trials for Neuropathic Traumatic Pain All trials for Pain NRS ≥ 4 All trials of Zarontin® (ethosuximide) and Stodal®

-Summary

Currently, it is established that the voltage-gated calcium channels modulate pain perception due to an influence on the neuronal transmission and excitability. In the past, attention has focused on the modulation of high voltage activated calcium channel. More recently, scientific interest has proven to the low voltage activated calcium channel, also called T-type channels. The data from the literature show significant involvement of these channels in the physiology of nociception and pathophysiology of acute and chronic pain. Moreover, in several animal pain models (acute, neuropathic, inflammatory), T-type channels inhibition alleviates painful behaviours.

Analgesics treatments available in clinic are ineffective in some patients with chronic pain (neuropathic, inflammatory) and often induce deleterious side effects. Thus, the clinical use of selective inhibitors of T-type channels could not only help the development of new therapies for the treatment of neuropathic pain (prevalence = 5-8 %), but also have a pharmaco-economic impact due to the low selling price of their inhibitor currently available: Zarontin®.

The purpose of this study is to assess the effectiveness of ethosuximide (Zarontin®) on the pain symptoms and quality of life in patients with peripheral neuropathic pain compared to a control group.

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+Detailed description

This is a multicentre, parallel-group, double-blind, randomised clinical trial comparing ethosuximide and inactive control for the treatment of peripheral neuropathic pain, assessed by numerical rating scale and quality of life questionnaire.

+Arms and interventions

ArmTypeInterventionsDescription
ethosuximideExperimentalDrug: Zarontin® (ethosuximide) and Stodal®The purpose of this study is to assess the effectiveness of ethosuximide (Zarontin®) on the pain symptoms and quality of life in patients with neuropathic traumatic pain compared to a control group.
control groupOtherDrug: Zarontin® (ethosuximide) and Stodal®The purpose of this study is to assess the effectiveness of ethosuximide (Zarontin®) on the pain symptoms and quality of life in patients with neuropathic traumatic pain compared to a control group.
  • Zarontin® (ethosuximide) and Stodal® (Drug), also known as Zarontin® (ethosuximide), administration: oral syrup using a graduated pipette. Duration of treatment: 42 days, Inactive substance: Stodal® administration: oral syrup using a graduated pipette. Duration of treatment: 42 days. Same dosage as Zarontin®

+Outcome measures

Primary outcomes

  • Assessment of the analgesic efficacy of ethosuximide in peripheral neuropathic pain patients [day 43]: Δ = score NRS (Day 0) - score NRS (D +43)

Secondary outcomes

  • Impact of ethosuximide on neuropathic pain [after day 43]
  • Quality of life [after day 43]
  • sleep and the overall impression of patients [after day 43]

+Eligibility

Sex: Male, ages: 18 Years to any

Inclusion Criteria:

* Age ≥ 18 years
* Traumatic neuropathy or post-surgical (excluding amputations) with Neuropathic -Pain Diagnostic DN4 ≥ 4 positive and IASP criteria
* ENS pain ≥ 4
* ALT, AST, PAL, normal GGT, creatinine <133μmol / L, hematocrit> 38%, β-HCG
* Patients affiliated to the French Social Security
* Patients with free and informed consent has been obtained
* Peripheral neuropathic pain with Neuropathic Pain Diagnostic DN4 ≥ 4 positive

Exclusion Criteria:

* Pregnancy or breastfeeding
* Diabetic neuropathy, post-herpetic neuralgia, cancer or chemotherapy-induced,
* Patients with impaired glucose tolerance,
* Medical and surgical history incompatible with the study,
* History of renal disease and / or liver,
* Addiction to alcohol and / or drugs,
* Taking antiepileptic family carboxamides and ethosuximide
* Use of St. John's wort,
* Allergy succinimides (ethosuximide, methsuximide, phensuximide)
* Psychotic disorders,
* Patients with epilepsy,
* Patient exclusion period, or the total allowable compensation exceeded
* Patients undergoing a measure of legal protection (guardianship, supervision ...)
* Central neuropathic pain
* Other chronic pain (osteoarthritis, arthritis, fibromyalgia…) with intensity greater than neuropathic pain

+Locations (1)

FacilityCityCountryStatus
CHU de Clermont-FerrandClermont-FerrandFrance

+Publications

  • Results publication: Kerckhove N, Pereira B, Soriot-Thomas S, Alchaar H, Deleens R, Hieng VS, Serra E, Lanteri-Minet M, Arcagni P, Picard P, Lefebvre-Kuntz D, Maindet C, Mick G, Balp L, Lucas C, Creach C, Letellier M, Martinez V, Navez M, Delbrouck D, Kuhn E, Piquet E, Bozzolo E, Brosse C, Lietar B, Marcaillou F, Hamdani A, Leroux-Bromberg N, Perier Y, Vergne-Salle P, Gov C, Delage N, Gillet D, Romettino S, Richard D, Mallet C, Bernard L, Lambert C, Dubray C, Duale C, Eschalier A. Efficacy and safety of a T-type calcium channel blocker in patients with neuropathic pain: A proof-of-concept, randomized, double-blind and controlled trial. Eur J Pain. 2018 Aug;22(7):1321-1330. doi: 10.1002/ejp.1221. Epub 2018 Apr 18. PMID 29577519
  • Results publication: Kerckhove N, Mallet C, Pereira B, Chenaf C, Duale C, Dubray C, Eschalier A. Assessment of the effectiveness and safety of Ethosuximide in the Treatment of non-Diabetic Peripheral Neuropathic Pain: EDONOT-protocol of a randomised, parallel, controlled, double-blinded and multicentre clinical trial. BMJ Open. 2016 Dec 16;6(12):e013530. doi: 10.1136/bmjopen-2016-013530. PMID 27986742

+Investigators

  • Alain ESCHALIER, Principal investigator, University Hospital, Clermont-Ferrand