MedDRA 10064697
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: • Age = 18 years • Patients with epiretinal gliosis and BCVA = 35 (according to ETDRS). • Written informed consent to participate in the study • Presence of an artificial intraocular lens • Ability to donate autologous platelets
Exclusion criteria
Exclusion criteria: • Patients with own lens • Treatment with intravitreal injections in the previous 3 months in the study eye • Pathological changes of the anterior segment of the eye affecting BCVA (corneal opacities or similar) • Acute inflammation in the study eye • advanced glaucoma with optic atrophy and central visual field defects in the study eye • wet form of age-related macular degeneration as well as advanced form of dry age-related macular degeneration (geographic atrophy) • presence of pregnancy
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| To investigate whether the intraoperative use of autologous platelet concentrate in patients with epiretinal gliosis and impending macular hole leads to better visual recovery than in patients without intraoperative platelet use. | — |
Secondary
| Measure | Time frame |
|---|---|
| • Comparison of retinal recovery on OCT between patients with and without intraoperative use from autologous platelet concentrate. • Comparison of visual recovery in patients with primary and secondary epiretinal gliosis. • Comparison of visual recovery in patients with diabetes mellitus and without. • Safety profile of intraoperative use of autologous platelet concentrate. | — |
Countries
Germany
Contacts
Augenklinik der Klinikum Chemnitz gGmbH