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Clinical Trial Summary

The goal of this double-blind prospective randomized clinical trial is to determine if the effect of intravenous erythropoietin is superior to the effect of intravenous methylprednisolone in cases of toxic optic neuropathy 4 weeks after therapeutic intervention. The main question it aims to answer: • Is there a difference in the visual recovery of toxic optic neuropathies treated with intravenous methylprednisolone in comparison with those treated with intravenous erythropoietin?


Clinical Trial Description

A double-blind prospective randomized clinical trial of treatment for toxic optic neuropathies comparing visual outcome of patients treated by standard treatment (intravenous methylprednisolone) vs intravenous erythropoietin. Enrollment: 18. Randomized groups (2) 1. Standard treatment (intravenous methylprednisolone) 2. Intravenous erythropoietin Masking: Double (participant and outcomes assessor) Participants won't be aware to which group they were assigned. Investigator in charge of assessing outcomes and analyzing data won't be aware to which group participants were assigned ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05748561
Study type Interventional
Source Asociación para Evitar la Ceguera en México
Contact Jorge Cárdenas-Belaunzarán, MD, MSc
Phone 5544600113
Email jorge.cardenas@apec.com.mx
Status Recruiting
Phase Phase 2/Phase 3
Start date April 5, 2022
Completion date April 5, 2024

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