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Systemic Erythropoietin Injection in Patients Having Optic Atrophy

A

Alexandria University

Status and phase

Completed
Phase 2
Phase 1

Conditions

Optic Atrophy

Treatments

Drug: Systemic erythropoietin injection

Study type

Interventional

Funder types

Other

Identifiers

NCT04680143
0304845

Details and patient eligibility

About

The purpose of this treatment trial is to study the effect of systemic erythropoietin in patients having optic atrophy.

Full description

The purpose of this treatment trial is to study the effect of systemic erythropoietin in patients having optic atrophy. The intervention is systemic erythropoietin injections (eprax 10000 IU subcutaneous twice daily for three days).

Follow up after one month and three months by recording visual acuity and electro physiological studies.

Enrollment

10 patients

Sex

All

Ages

18 to 80 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Post papilledemic optic atrophy patients

Exclusion criteria

  • Refuse to give an informed consent

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

10 participants in 1 patient group

Systemic erythropoietin injections
Experimental group
Description:
The study included 10 patients diagnosed as post papilledemic optic atrophy
Treatment:
Drug: Systemic erythropoietin injection

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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