UnknownNot Applicable

Outcome After Descemet Membrane Endothelial Keratoplasty (DMEK) and Ultra-thin Descemet Stripping Automated Endothelial Keratoplasty (DSAEK)

Germany200 participantsStarted 2012-09

Plain-language summary

The purpose of this study is evaluate the outcome after posterior lamellar keratoplasty (DMEK and Ultra-thin DSAEK) for corneal transplantation.

Who can participate

Age range18 Years

SexALL

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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.

Inclusion Criteria: * Male or female aged 18 or older * Scheduled to undergo endothelial keratoplasty * Able to provide written informed consent. Exclusion Criteria: * Age less than 18 years

What they're measuring

Visual acuity (change from baseline)

Timeframe: 1, 3, 6, and 12 months and annually

Trial details

NCT IDNCT02020044

SponsorCharite University, Berlin, Germany

Sponsor typeOTHER

Study typeINTERVENTIONAL

Primary completion2015-12

Contact for this trial

Anna-Karina Maier, MD

anna-karina.maier@charite.de

View on ClinicalTrials.gov More Fuchs' Endothelial Corneal Dystrophy trials