Corneal Endothelium Delivery Instrument
Status unconfirmed · Phase 2
Conditions studied: Corneal Transplantation
In brief
The purpose of this study is to determine whether the surgical outcomes in patients undergoing Descemet's Stripping Endothelial Keratoplasty (DSEK) are improved with the use of an insertion device over the traditional forceps insertion method.
Key facts
- Study ID
- NCT00874835
- Run by
- Ocular Systems, Inc.
- People needed
- 100
- Starts
- 2009-03-01
- Expected to finish
- 2010-10-01
- Last updated by the study team
- 2010-05-07
Who can join
Age: 45 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients with Fuchs endothelial dystrophy or bullous keratopathy determined to need a corneal transplant for visual restoration.
Where it is running
- Wake Forest University Eye Center — Winston-Salem, North Carolina, United States
Full record on ClinicalTrials.gov
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