Skip to content

Edaravone in the Treatment of Optic Neuritis

Edaravone in the Treatment of Optic Neuritis

Status
Recruiting
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05540262
Enrollment
50
Registered
2022-09-14
Start date
2022-01-15
Completion date
2025-12-31
Last updated
2025-02-27

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

Conditions

Optic Neuritis

Brief summary

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

Edaravone injection 30mg three times a day

Sponsors

First Affiliated Hospital of Guangxi Medical University
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE

Eligibility

Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No

Inclusion criteria

1. Chinese patients aged ≥18 with anti-aquaporin-4 antibody-positive optic neuritis 2. Patients with a first episode of optic neuritis in either eye 3. First symptoms of optic neuritis ≤30 days prior to the first administration of edaravone

Exclusion criteria

1. Myopia over 6 diopters 2. Refractive media opacity affecting assessment of retinal layers and/or visual acuity

Design outcomes

Primary

MeasureTime frameDescription
Best-corrected visual acuity18 monthsBest-corrected visual acuity will be measured by Illiterate Echart.

Secondary

MeasureTime frameDescription
Ganglion cell-inner plexiform layer18 monthsGanglion cell-inner plexiform layer will be measured by optical coherence tomography.
Peripapillary retinal nerve fiber layer18 monthsPeripapillary retinal nerve fiber layer will be measured by optical coherence tomography.

Countries

China

Outcome results

None listed

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