Fuchs Endothelial Corneal Dystrophy Clinical Trials
30 clinical trials for Fuchs Endothelial Corneal Dystrophy across international registries, including 10 currently recruiting participants. Compare status, phase, eligibility criteria and locations.
- Prognosis of Posterior Lamellar Keratoplasty — RECRUITING
- Effect of Descemet Membrane Polishing in Fuchs Endothelial Corneal Dystrophy — RECRUITING · NA
- Effect of Donor Diabetes and Other Factors on Corneal Transplant Endothelial Cell Loss and Success at 5 Years — RECRUITING · NA
- Influence of Supine Positioning on the Outcomes After Descemet Membrane Endothelial Keratoplasty (DMEK) — RECRUITING · NA
- DT-168 in Keratoplasty Patients With Fuchs Endothelial Corneal Dystrophy — RECRUITING · PHASE2
- SUCCESS Score Validation in Fuchs Dystrophy — RECRUITING
- Targeting Reactive Oxygen Species Production as a Novel Therapeutic in Fuch's Endothelial Corneal Dystrophy — RECRUITING · PHASE2
- Comparison of Outcomes Between Femtosecond Laser-Assisted and Conventional Phacoemulsification in Fuchs Endothelial Corneal Dystrophy Patients With Cataracts — RECRUITING
- The Effect of Topical Rho-kinase Inhibitors on Corneas of Patients With Fuchs Endothelial Corneal Dystrophy — RECRUITING
- A DOUBLE-MASKED, RANDOMIZED, PLACEBO-CONTROLLED, PARALLEL-GROUP, 12-WEEK ADMINISTRATION WITH TWO-WEEK GRADUAL DOSE TAPER PHASE AND 38-WEEK FOLLOW-UP PHASE, PHASE 3 STUDY TO INVESTIGATE THE SAFETY AND EFFICACY OF RIPASUDIL (K-321) EYE DROPS AFTER DESCEMETORHEXIS IN SUBJECTS WITH FUCHS ENDOTHELIAL CORNEAL DYSTROPHY — RECRUITING · PHASE3
- Postoperative CCT in FECD vs. Non-FECD — NOT_YET_RECRUITING
- A Multicenter Study Assessing the Efficacy and Safety of STN1010904 Ophthalmic Suspension 0.03% and 0.1% Compared With Vehicle in Subjects With Fuchs Endothelial Corneal Dystrophy (FECD) — COMPLETED · PHASE2
- A Study to Evaluate the Safety and Efficacy of K-321 Eye Drops After Descemetorhexis in Participants With Fuchs Endothelial Corneal Dystrophy (FECD) — COMPLETED · PHASE3
- Partial Range Of Field IOLs in DMEK-Enabled Procedures — NOT_YET_RECRUITING · NA
- Assessment of Corneal Endothelial Function Following Hypoxic Stress — WITHDRAWN · PHASE1
- A Study to Investigate the Safety and Efficacy of K-321 Eye Drops After Simultaneous Cataract Surgery and Descemetorhexis in Participants With Fuchs Endothelial Corneal Dystrophy (FECD) — COMPLETED · PHASE3
- Prevalence of Fuchs Endothelial Corneal Dystrophy in a Population of Dermatology Patients. — COMPLETED
- A Phase IIa, Randomized, Double-Masked, Placebo-Controlled, Parallel-Group, Multicenter Study Assessing the Efficacy and Safety of STN1010904 Ophthalmic Suspension 0.03% and 0.1% Compared with Vehicle in Subjects with Fuchs Endothelial Corneal Dystrophy (FECD) - PHANTOM Study — OTHER · PHASE2
- A Double-Masked, Randomized, Placebo-Controlled, Parallel-Group, 12-Week Administration With Two-Week Gradual Dose Taper Phase and 38-Week Follow-Up Phase, Phase 3 Study to Investigate the Safety and Efficacy of Ripasudil (K-321) Eye Drops After Descemetorhexis in Subjects with Fuchs Endothelial Corneal Dystrophy — OTHER · PHASE3
- Study of Safety and Tolerability of EO2002 in the Treatment of Corneal Edema — COMPLETED · PHASE1
- Study to Investigate the Safety and Efficacy of K-321 in Patients With Fuchs Endothelial Corneal Dystrophy (FECD) Following Descemetorhexis — COMPLETED · PHASE2
- A Phase 1/ Phase 2 Study of TTHX1114(NM141) — COMPLETED · PHASE1
- A DOUBLE-MASKED, RANDOMIZED, PLACEBO-CONTROLLED, PARALLEL-GROUP, 12-WEEK ADMINISTRATION WITH TWO-WEEK GRADUAL DOSE TAPER PHASE AND 38-WEEK FOLLOW-UP PHASE, PHASE 3 STUDY TO INVESTIGATE THE SAFETY AND EFFICACY OF RIPASUDIL (K-321) EYE DROPS AFTER SIMULTANEOUS CATARACT SURGERY AND DESCEMETORHEXIS IN SUBJECTS WITH FUCHS ENDOTHELIAL CORNEAL DYSTROPHY — COMPLETED · PHASE3
- Analysis of the Genotype/Phenotype Relationship in the Fuchs' Corneal Endothelial Dystrophy in France. — COMPLETED
- Predictive Factors of Graft Detachment Following Dmek — COMPLETED
- Study With QR-504a to Evaluate Safety, Tolerability & Corneal Endothelium Molecular Biomarker(s) in Subjects With FECD3 — WITHDRAWN · PHASE1
- The Postoperative Head Position as a Predictor of the Surgical Outcome After DMEK — OTHER
- Study of Endothelial Keratoplasty Outcomes — COMPLETED · NA
- Fuchs' Endothelial Dystrophy: Clinical Characteristics, Treatment Outcome, and Pathology — COMPLETED · NA
- Outcome After Descemet Membrane Endothelial Keratoplasty (DMEK) and Ultra-thin Descemet Stripping Automated Endothelial Keratoplasty (DSAEK) — OTHER · NA
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