Edaravone in the Treatment of Optic Neuritis

Trial statusRecruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-70
SponsorFirst Affiliated Hospital of Guangxi Medical University

About this trial

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.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

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

Disqualifiers

Myopia over 6 diopters

Refractive media opacity affecting assessment of retinal layers and/or visual acuity

Trial design

Design model

Single group

Treatments tested in this trial

  • Edaravone

    Drug

    Edaravone injection 30mg three times a day

Treatment groups

50 Participants
are divided into 1 treatment group
Group A: EdaravoneExperimental treatment 1 intervention

Trial outcomes

Primary outcomes

1

Best-corrected visual acuity

Best-corrected visual acuity will be measured by "Illiterate E"chart.

Time frame
18 months

Secondary outcomes

1

Ganglion cell-inner plexiform layer

Ganglion cell-inner plexiform layer will be measured by optical coherence tomography.

Time frame
18 months
2

Peripapillary retinal nerve fiber layer

Peripapillary retinal nerve fiber layer will be measured by optical coherence tomography.

Time frame
18 months

Other outcomes

Sponsors and contacts

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