Alexandria Faculty of Medicine
Alexandria, Egypt
NCT Number: NCT04680143
The purpose of this treatment trial is to study the effect of systemic erythropoietin in patients having optic atrophy.
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Notify Me18 year–80 year
All sexes
Interventional
Phase 1 / Phase 2
Alexandria, Egypt
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.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Systemic erythropoietin injections (eprax 10000 IU subcutaneous twice daily for three days).
Other names: Eprax 10000
Time frame: 3 months
VIsual acuity assessed at the follow up
Time frame: 3 months
Pattern visual evoked Potential .in both eyes to use data of the normal fellow eye as patients' internal control
Time frame: 3 months
Pattern electroretinogram in both eyes to use data of the normal fellow eye as patients' internal control
Alexandria University
Other
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