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Clinical Trial Summary

To evaluate the impact of preoperative corneal thickness on visual outcomes following Descemet's stripping endothelial keratoplasty (DSAEK) or Descemet membrane endothelial keratoplasty (DMEK)


Clinical Trial Description

Patients underwent DSAEK or DMEK for endothelial dysfunction, from October 2013 to November 2016. Patients aged > 18 years and with an indication for posterior lamellar graft surgery, such as Fuchs dystrophy, were included. Exclusion criteria included a history of penetrating keratoplasty in the study eye and a need for a penetrating keratoplasty following endothelial graft failure. Visual acuity, central corneal thickness (CCT) and graft thickness were measured preoperatively, and at postoperative day 7 and months 1, 3 and 6. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03355911
Study type Observational
Source Centre Hospitalier Régional Metz-Thionville
Contact
Status Completed
Phase N/A
Start date October 1, 2016
Completion date May 30, 2017