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Subcutaneous Injection of Erythropoietin on Visual Functions in Patients With Late Onset Optic Neuropathy

A

Alexandria University

Status and phase

Completed
Phase 2
Phase 1

Conditions

Optic Neuropathy

Treatments

Drug: erythropoietin

Study type

Interventional

Funder types

Other

Identifiers

NCT04469777
0304649

Details and patient eligibility

About

This study aimed to investigate the therapeutic effect of subcutaneous erythropoietin in the management of late stage optic neuropathy.

Full description

Injury of the optic nerve or optic neuropathy is one of the most common causes of vision loss. This study aimed to investigate the therapeutic effect of subcutaneous erythropoietin in the management of late stage optic neuropathy.

Enrollment

20 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with late stage optic neuropathy (1 month to 12 months after onset of optic neuropathy due to late referral of the cases)

Exclusion criteria

  • Patients with perforating ocular injuries were excluded.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

20 participants in 1 patient group

Systemic erythropoietin injections
Experimental group
Description:
20 patients diagnosed as late onset optic neuropathy that were attending Alexandria main university hospital.Systemic erythropoietin injections (eprax 10000 IU subcutaneous twice daily for three days).
Treatment:
Drug: erythropoietin

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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