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Recruiting NCT05540262

Edaravone in the Treatment of Optic Neuritis

No phase Interventional Optic Neuritis

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Edaravone.
Who it may be relevant to
Registry conditions: Optic Neuritis. Basic parameters: 18 years — 70 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
China
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →

Overview

Edaravone has demonstrated a beneficial effect in promoting remyelination and protecting axons in animals with NMOSD. The researchers posit that edaravone may enhance visual outcomes in patients with aquaporin-4 antibody-positive optic neuritis.

Interventions

  • Drug Edaravone
    Edaravone injection 30mg three times a day

Primary outcome measures

  • Best-corrected visual acuity [Time frame: 18 months]
Secondary outcome measures (2)
  • Ganglion cell-inner plexiform layer [Time frame: 18 months]
  • Peripapillary retinal nerve fiber layer [Time frame: 18 months]

Eligibility criteria

Inclusion criteria

  • Chinese patients aged ≥18 with anti-aquaporin-4 antibody-positive optic neuritis
  • Patients with a first episode of optic neuritis in either eye
  • First symptoms of optic neuritis ≤30 days prior to the first administration of edaravone

Exclusion criteria

  • Myopia over 6 diopters
  • Refractive media opacity affecting assessment of retinal layers and/or visual acuity

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Healthy volunteers: No

Study design

Allocation
N/A
Model
Single group
Masking
Open label
Primary purpose
Treatment

Study locations

China · 1 center
  • Yi Du — Nanning

Identifiers

NCT: NCT05540262 · GXEDAON1.0

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗