Bullous Keratopathy

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Review clinical trials related to Bullous Keratopathy. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

Utilization of Residual Donor Tissue for Regrafting in Bullous Keratopathy After Corneal Transplantation

Postoperative endothelial cell loss following Descemet stripping endothelial keratoplasty (DSEK) remains a well-recognized clinical concern, with long-term follow-up demonstrating approximately 50% reduction in endothelial cell density by 5 years. Compounding this challenge, the critical shortage of corneal donors has severely limited the expansion of corneal transplantation programs in developing countries. In conventional penetrating keratoplasty, only the central 7-mm optical zone is typically harvested, whereas the peripheral donor tissue-whose endothelial cells are believed to exhibit superior viability-is routinely discarded. To address these limitations, we describe the first-in-human use of three residual peripheral donor tissue segments, obtained after conventional keratoplasty, which were combined to perform corneal endothelial transplantation. This innovative approach substantially enhanced donor tissue utilization. Postoperatively, the patient achieved sustained corneal transparency with visual acuity improving from 20/500 to 20/50. Notably, the intersegmental gaps resolved progressively over time. Extending this proof-of-concept case, we subsequently investigated the long-term stability and safety of residual donor tissue endothelial keratoplasty for bullous keratopathy, with comprehensive evaluation of postoperative visual acuity, intraocular pressure, corneal endothelial cell density, and refractive outcomes. This study aims to establish evidence-based support for the safety and efficacy of utilizing residual graft tissue in corneal endothelial transplantation.

Participants needed: 20
Trial details
Age: 18+Biological sex: AllType: InterventionalSponsor: Zhongshan Ophthalmic Center, Sun Yat-sen UniversityUpdated: Oct 2, 2026Locations: 1
Eligibility criteria

Patients with bullous keratopathy of various etiologies, with a corneal thicknes... [+2]

Loss of vision in the fellow eye. [+14]

Status: Recruiting

Simple Non-cultured Endothelial Cell Therapy for Corneal Endothelial Dysfunction

Assessment of safety and efficacy of cell injection therapy generated using non-cultured human corneal endothelial cells in treating corneal endothelial dysfunction

Participants needed: 20
Trial details
Phase: Phase 1Age: 18-80Biological sex: AllType: InterventionalSponsor: Singapore Eye Research InstituteUpdated: Jul 17, 2026Locations: 1
Eligibility criteria

Severe forms or late-stage presentation of corneal decompensation with severe co... [+9]

Status: Recruiting

Study to Assess Safety and Tolerability of Multiple Doses of EO2002

The goal of this clinical study is to assess the safety of multiple intracameral injections of EO2002 with and without topical Ripasudil.

Participants needed: 12
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Asociación para Evitar la Ceguera en MéxicoUpdated: Dec 8, 2025Locations: 1
Eligibility criteria

Age ≥ 18 years. [+2]

Other corneal disease [+10]

Status: Recruiting

Safety and Efficacy of Tissue Engineered Endothelial Keratoplasty

Assessment of safety and efficacy of tissue-engineered corneal endothelial graft material generated using cultured human corneal endothelial cells for tissue-engineered endothelial keratoplasty (TE-EK).

Participants needed: 30
Trial details
Phase: Phase 1Age: 21-80Biological sex: AllType: InterventionalSponsor: Singapore Eye Research InstituteUpdated: Sep 12, 2025Locations: 1
Eligibility criteria

Fuchs' endothelial dystrophy [+1]

Severe forms or late stage presentation of corneal decompensation with severe co... [+9]