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Fuchs' Endothelial Dystrophy clinical trials

View clinical trials related to Fuchs' Endothelial Dystrophy.

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NCT ID: NCT05052554 Withdrawn - Corneal Diseases Clinical Trials

Study With QR-504a to Evaluate Safety, Tolerability & Corneal Endothelium Molecular Biomarker(s) in Subjects With FECD3

Fuchs Focus
Start date: August 10, 2021
Phase: Phase 1
Study type: Interventional

PQ-504a-001 (Fuchs Focus) is an open-label, single-dose, exploratory study to evaluate safety, tolerability, and corneal endothelium molecular biomarker(s) in subjects with Fuchs Endothelial Corneal Dystrophy with Trinucleotide Repeat Expansion in the TCF4 gene (FECD3).

NCT ID: NCT04018417 Withdrawn - Clinical trials for Fuchs' Endothelial Dystrophy

Evaluation of Amphotericin B in Optisol-GS for Prevention of Post-Keratoplasty Fungal Infections.

Start date: July 3, 2019
Phase: Phase 2/Phase 3
Study type: Interventional

With the increasing popularity of endothelial keratoplasty, a coincident increase in the rate of fungal infections post-keratoplasty has been seen in the United States. In this study, the eye bank will harvest pairs of donor corneas and randomize one cornea from each pair to be stored in Optisol-GS per Eye Bank Association of America guidelines. The eye bank will add amphotericin B 0.255 μg/mL (antifungal) to the storage solution for the mate cornea. The study donor corneas will be assigned to participants who are scheduled to undergo Descemet membrane endothelial keratoplasty. The surgeons, participants, and evaluators will remain masked regarding the donor cornea storage solution assignment. The participants will be followed for 6 months.

NCT ID: NCT02109276 Withdrawn - Cataracts Clinical Trials

Study of the Effect of Aspheric Lenses in Patients With Fuch's Dystrophy

Start date: April 2014
Phase: N/A
Study type: Interventional

The proposed study will recruit patients with mild to moderate Fuch's dystrophy who need cataract surgery alone. They will be randomly assigned to receive either spheric or aspheric lenses. If both eyes of a patient need surgery, we will implant the same type of lens in each eye in order to prevent imbalanced vision. We will measure their contrast sensitivity and higher order aberrations before surgery and 3 months after surgery. We will compare the change in these values between the two groups.