corneal dystrophy
corneal dystrophy
Explore linked clinical trials. Standard reference: MONDO:001810234 results · Page 1 of 2
Clinical trials
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| Trial | Conditions | Status | Phase | Updated | More info | NCT ID |
|---|---|---|---|---|---|---|
| Study of EO2002 in Subjects With Corneal Edema Secondary to Corneal Endothelial Dysfunction | Chandler syndrome, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Corneal Endothelial Cell Loss, Corneal Endothelial Dystrophy 1, Eye Diseases, Hereditary, Eye Manifestations, Fuchs' endothelial dystrophy, Pathologic Processes, Pathological Conditions, Signs and Symptoms, Postoperative Complications, Signs and Symptoms, congenital hereditary endothelial dystrophy of cornea, corneal disorder, corneal dystrophy, corneal edema, eye disorder, hereditary disease | Recruiting | Phase 2 | 2026-10-09 | NCT07729137 | |
| A Study to Test the Diagnostic Potential of Brillouin Microscopy for Corneal Ectasia | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Dilatation, Pathologic, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, Pathological Conditions, Anatomical, Pathological Conditions, Signs and Symptoms, corneal disorder, corneal dystrophy, eye disorder, hereditary disease, keratoconus | Recruiting | Not stated | 2026-10-08 | NCT02118922 | |
| DT-168 in Keratoplasty Patients With Fuchs Endothelial Corneal Dystrophy | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, eye disorder, hereditary disease | Recruiting | Phase 2 | 2026-09-28 | NCT07024693 | |
| The Belgian Endothelial Surgical Transplant of the Cornea | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, bullous keratopathy, corneal disorder, corneal dystrophy, corneal edema, eye disorder, hereditary disease | Active, not recruiting | Not applicable | 2026-09-14 | NCT05436665 | |
| Safety and Efficacy Study of GEB-101 Injection in Subjects With TGFBI-related Corneal Dystrophy | Amyloid Neuropathies, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Nutritional and Metabolic Diseases, Thiel-Behnke corneal dystrophy, amyloidosis, corneal disorder, corneal dystrophy, eye disorder, familial amyloid neuropathy, hereditary amyloidosis, hereditary disease, inborn errors of metabolism, inherited neurodegenerative disorder, metabolic disease, nervous system disorder, neurodegenerative disease, neuromuscular disease, peripheral nervous system disorder, proteostasis deficiencies | Not yet recruiting | Phase 1 / Phase 2 | 2026-09-10 | NCT07750678 | |
| The Effect of Topical Rho-kinase Inhibitors on Corneas of Patients With Fuchs Endothelial Corneal Dystrophy | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, cataract, corneal disorder, corneal dystrophy, corneal edema, eye disorder, glaucoma, hereditary disease, lens disorder, ocular hypertension | Enrolling by invitation | Not stated | 2026-09-09 | NCT06969586 | |
| Targeting Reactive Oxygen Species Production as a Novel Therapeutic in Fuch's Endothelial Corneal Dystrophy | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, eye disorder, hereditary disease | Recruiting | Phase 2 | 2026-09-02 | NCT04440280 | |
| Partial Range Of Field IOLs in DMEK-Enabled Procedures | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, cataract, corneal disorder, corneal dystrophy, eye disorder, hereditary disease, lens disorder | Not yet recruiting | Not applicable | 2026-08-25 | NCT07441616 | |
| Descemet Endothelial Thickness Comparison Trial II | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, eye disorder, hereditary disease | Recruiting | Phase 3 | 2026-08-17 | NCT05275972 | |
| Postoperative CCT in FECD vs. Non-FECD | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, cataract, corneal disorder, corneal dystrophy, eye disorder, hereditary disease, lens disorder | Not yet recruiting | Not stated | 2026-08-10 | NCT07731945 | |
| Fresh Corneal Lenticule Implantation in Macular Corneal Distrophy With Relex Smile Surgery | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, corneal disorder, corneal dystrophy, eye disorder, hereditary disease, macular corneal dystrophy | Enrolling by invitation | Not applicable | 2026-07-29 | NCT04642729 | |
| Prognosis of Posterior Lamellar Keratoplasty | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, eye disorder, hereditary disease | Recruiting | Not stated | 2026-06-24 | NCT06859411 | |
| National Ophthalmic Genotyping and Phenotyping Network (eyeGENE (Registered Trademark)), Stage 3 - Expansion of DNA and Data Repositories for Rare Inherited Ophthalmic Diseases | Congenital Abnormalities, Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Abnormalities, Eye Diseases, Hereditary, Nutritional and Metabolic Diseases, Skin and Connective Tissue Diseases, albinism, aniridia, blue cone monochromacy, corneal disorder, corneal dystrophy, eye disorder, hereditary disease, hereditary skin disorder, hypopigmentation of the skin, inborn disorder of amino acid metabolism, inborn errors of metabolism, iris disorder, macular degeneration, metabolic disease, retinal degeneration, retinal disorder, skin disorder, skin pigmentation disorder, uveal disorder, vitelliform macular dystrophy, vitiligo | Recruiting | Not stated | 2026-06-09 | NCT06491615 | |
| Effect of Descemet Membrane Polishing in Fuchs Endothelial Corneal Dystrophy | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, eye disorder, hereditary disease | Recruiting | Not applicable | 2026-05-26 | NCT07539012 | |
| Analysis of the Genotype/Phenotype Relationship in the Fuchs' Corneal Endothelial Dystrophy in France | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Corneal Dystrophy, Posterior Polymorphous, 1, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, eye disorder, hereditary disease | Recruiting | Not stated | 2026-05-06 | NCT05742321 | |
| Plasma Rich in Growth Factors in Corneal Endothelial Transplantation | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, corneal edema, eye disorder, hereditary disease | Recruiting | Not applicable | 2026-04-09 | NCT06261346 | |
| Effect of Donor Diabetes and Other Factors on Corneal Transplant Endothelial Cell Loss and Success at 5 Years | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, eye disorder, hereditary disease | Enrolling by invitation | Not applicable | 2026-02-27 | NCT07217249 | |
| Influence of Supine Positioning on the Outcomes After Descemet Membrane Endothelial Keratoplasty (DMEK) | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, eye disorder, hereditary disease | Recruiting | Not applicable | 2026-01-28 | NCT07373821 | |
| PVEK Corneal Implant For Treatment of Corneal Edema | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, corneal edema, eye disorder, hereditary disease | Recruiting | Phase 1 | 2026-01-12 | NCT07325097 | |
| Study to Assess Safety and Tolerability of Multiple Doses of EO2002 | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Corneal Dystrophy, Posterior Polymorphous, 1, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, bullous keratopathy, corneal disorder, corneal dystrophy, corneal edema, corneal endothelial dystrophy, eye disorder, hereditary disease | Recruiting | Phase 1 | 2025-12-08 | NCT05636579 | |
| SUCCESS Score Validation in Fuchs Dystrophy | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, eye disorder, hereditary disease | Recruiting | Not stated | 2025-12-04 | NCT07265388 | |
| High Resolution, High-speed Multimodal Ophthalmic Imaging | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Nutritional and Metabolic Diseases, age-related macular degeneration, brain disorder, cardiovascular disorder, central nervous system disorder, cerebrovascular disorder, corneal disorder, corneal dystrophy, diabetes mellitus, dry eye syndrome, endocrine system disorder, eye disorder, glaucoma, glucose metabolism disease, hereditary disease, hypertensive disorder, inherited retinal dystrophy, injury, keratoconus, lacrimal apparatus disorder, macular degeneration, macular retinal edema, metabolic disease, nervous system disorder, ocular hypertension, retinal degeneration, retinal detachment, retinal disorder, retinitis pigmentosa, stroke disorder, vascular disorder | Recruiting | Not applicable | 2025-11-18 | NCT04129021 | |
| The OPTIMISE Study | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, eye disorder, hereditary disease | Recruiting | Phase 4 | 2025-10-06 | NCT05716945 | |
| Safety and Efficacy of Tissue Engineered Endothelial Keratoplasty | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, bullous keratopathy, corneal disorder, corneal dystrophy, eye disorder, hereditary disease | Recruiting | Phase 1 | 2025-09-12 | NCT04319848 | |
| OCT in Fuchs' Dystrophy | Congenital, Hereditary, and Neonatal Diseases and Abnormalities, Eye Diseases, Hereditary, Fuchs' endothelial dystrophy, corneal disorder, corneal dystrophy, eye disorder, hereditary disease | Recruiting | Not stated | 2025-09-09 | NCT04258787 |