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Not yet recruiting Not applicable NCT07539012

Effect of Descemet Membrane Polishing in Fuchs Endothelial Corneal Dystrophy

No applicable phase (e.g. observational)
Conditions: Fuchs Endothelial Corneal Dystrophy

Sponsor: Centre Hospitalier Universitaire de Saint Etienne

trial.available_in: БГ
Overview
Fuchs endothelial corneal dystrophy (FECD) is the leading indication for corneal transplantation worldwide. It is characterized by the accumulation of guttae and progressive loss of corneal endothelial cells, leading to corneal edema and visual impairment. Endothelial keratoplasty remains the standard treatment; however, graft shortages have driven the development of cell-based therapies involving the injection of cultured endothelial cells. A key unresolved issue is whether removal of the pathological endothelium prior to injection improves cell adhesion. Clinical data are limited and sometimes contradictory, particularly regarding endothelial polishing. The actual effectiveness of this procedure in removing guttae and enhancing the survival of injected cells remains uncertain. Therefore, an in vivo clinical evaluation is required to assess its impact on guttae removal.
Who can participate
Inclusion Criteria: * Patient affiliated with or entitled to a social security scheme * Patient scheduled for endothelial keratoplasty for Fuchs endothelial corneal dystrophy * Patient having received full information and having provided written informed consent Exclusion Criteria: * Pregnant women * Adults under legal protection (guardianship/curatorship) or unable to provide informed consent
Interventions
Fuchs Polishing
PROCEDURE
Locations 5
France (5)
Hopital de Mercy
Metz , Metz
Cochin Hospital
Paris , Paris
Hôpital Fondation Rothschild
Paris , Paris
Centre Hospitalier Universitaire de Rouen
Rouen , Rouen
CHU de Saint-Etienne
Saint-Etienne , France
Technical details
Status
Not yet recruiting
Phase
Not applicable
Study type
INTERVENTIONAL
Sex
Male and female
Minimum age
18 Years
Healthy volunteers
No
Start date
01.05.2026
Completion date
01.03.2027
Registry ID
NCT07539012
Source
clinicaltrials.gov
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