The purpose of this study is evaluate the outcome after posterior lamellar keratoplasty (DMEK and Ultra-thin DSAEK) for corneal transplantation.
Study Type
INTERVENTIONAL
Allocation
NA
Purpose
TREATMENT
Masking
NONE
Enrollment
200
Department of Ophthalmology, Charité - Universitätsmedizin Berlin
Berlin, State of Berlin, Germany
RECRUITINGVisual acuity (change from baseline)
Time frame: 1, 3, 6, and 12 months and annually
Endothelial cell density (change from baseline)
Time frame: 1, 3, 6, and 12 months and annually
Intraocular pressure (change from baseline)
Time frame: 1, 3, 6, and 12 months and annually
Manifest refraction (change from baseline)
Time frame: 1, 3, 6, 12 months and annually
corneal pachymetry (change from baseline)
Time frame: 1, 3, 6, 12 months and annually
Quality of Life, NEI-VFQ 25 (change from baseline)
Questionnaire
Time frame: 3, 12 months, annualy
corneal topography (change from baseline)
Time frame: 1, 3, 6, and 12 months and annually
Anterior Segment OCT of cornea and anterior chamber angle (change from baseline)
Time frame: 1, 3, 6, and 12 months and annually
postoperative Medication (change from baseline)
Time frame: 1,3,6 and 12 months and annually
Histological Sample of Recipient's Descemet Membrane
Recipient's Descemet Membrane
Time frame: intraoperative
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