ENDOTHELION Study Group: Effect of Bosentan in NAION Patients

Last updated: July 4, 2022
Sponsor: University Hospital, Grenoble
Overall Status: Active - Recruiting

Phase

3

Condition

Cardiac Ischemia

Treatment

N/A

Clinical Study ID

NCT02377271
2014-000848-14
  • Ages > 50
  • All Genders

Study Summary

Acute ischemic optic neuropathy are the second leading cause of optic neuropathy after glaucoma in the population aged over 50 years. The visual prognosis of the condition is unfavorable in the great majority of cases, with significant effects on the visual field and vision. The severity of the unilateral condition is also associated with bilateralization in 15% at 5 years. There is no effective treatment for the acute phase of the disease or to reduce the rate of bilateralization. In this context, it is essential to develop new therapeutic strategies in the acute phase of the disease to reduce the anatomical optic nerve damage.

Eligibility Criteria

Inclusion

Inclusion Criteria:

  • Non arteritic ischemic optic neuropathy (NAION) with onset < 21 days
  • Age ≥ 50 years old
  • Signed informed consent form
  • Patients affiliated with a national health insurance scheme or beneficiaries of such ascheme

Exclusion

Exclusion Criteria:

  • Pregnant women, women in labour or breast-feeding mother
  • Patients with other acute or chronic intercurrent ocular pathology interfering withvisual acuity or visual field (diabetes, drug-induced or other retinopathy, otheroptic neuropathy including uni- or contralateral glaucoma and/or intraocular pressure > 30 mmHg, advanced cataract, corneal opacities, amblyopia < 5/10, severe myopia > -6diopters, retinal disease)
  • Simultaneous bilateral NAAION, 1 month apart or less
  • Signs that may raise suspicion of other inflammatory neuropathy: arterial NAAION (Horton's disease), pain on eye movement or any signs suggestive of optic neuritis,known diagnosis of multiple sclerosis, history of inflammatory optic neuropathy (homo-or ipsi-lateral). A temporal artery biopsy should be performed if there are symptomssuggestive of Horton's disease, or if there is pale and/or diffuse edema, orobliteration of the associated central retinal artery.
  • Patients with systolic blood pressure below 100 mmHg
  • Patient with orthostatic hypotension (20 mmHg drop in SBP and/or 10 mmHg drop in DBPwhen moving to a standing position)
  • Neurological history of vascular or tumour-related changes to the visual field orother optic neuropathy
  • Systemic inflammatory disease
  • Known allergy to bosentan
  • Patients with moderate to severe hepatic impairment (Child-Pugh class B or C), biliarycirrhosis (serum levels of liver aminotransferases, aspartate aminotransferases (ASAT)and/or alanine aminotransferases (ALAT), greater than three times the upper limit ofnormal, bilirubin greater than twice normal)
  • Estimated glomerular filtration rate (GFR) < 30 ml/min/1.73 m2
  • Patients treated with drugs whose efficacy may be reduced by activation of cytochromeP450, 2C9, 3A4 and 2C19 isoenzymes
  • Patients treated with amiodarone
  • Patient treated with systemic corticosteroids (background treatment or treatmentinitiated at the time of NAAION diagnosis)
  • Person deprived of liberty by judicial or administrative decision, adult protected bylaw, hospitalized person
  • Ongoing participation in another clinical research study or in the exclusion period ofanother clinical study

Study Design

Total Participants: 86
Study Start date:
August 01, 2015
Estimated Completion Date:
December 31, 2025

Study Description

The main objective of our study will be to compare the treatment with bosentan to placebo for 8 weeks for recovery anatomical criteria (RFNL in OCT, optic atrophy) and functional (visual acuity, visual field). The primary endpoint will be the improvement of the visual field, a major criterion of the affected visual function in this disease.

The evaluation of bosentan will mainly after 8 weeks of treatment in order to assess the effectiveness of drug treatment in the absence of continuous positive airway pressure (set up after three months if necessary, feasible confounding factor for the evaluation of results ), the period of three months is sufficient to assess the anatomical and functional recovery (disappearance of papilledema).

Connect with a study center

  • University Hospital of Angers

    Angers, 49100
    France

    Active - Recruiting

  • University Hospital of Bordeaux

    Bordeaux, 33000
    France

    Terminated

  • CHU de Grenoble

    Grenoble, 38043
    France

    Active - Recruiting

  • University Hospital of Grenoble Michallon

    Grenoble, 38043
    France

    Active - Recruiting

  • University Hospital of Lyon

    Lyon, 69003
    France

    Site Not Available

  • Centre National d'Ophtalmologie XV-XX

    Paris,
    France

    Active - Recruiting

  • Ophtalmological fondation of Rothschild + Bichat Hospital

    Paris, 75019
    France

    Active - Recruiting

  • University hospital of Saint-Etienne

    Saint-Etienne, 42055
    France

    Active - Recruiting

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