Simple Non-cultured Endothelial Cell Therapy for Corneal Endothelial Dysfunction
Recruiting now · Phase 1
Conditions studied: Bullous Keratopathy, Corneal Endothelial Dystrophy
In brief
Assessment of safety and efficacy of cell injection therapy generated using non-cultured human corneal endothelial cells in treating corneal endothelial dysfunction
Key facts
- Study ID
- NCT07711561
- Run by
- Singapore Eye Research Institute
- People needed
- 20
- Starts
- 2026-06-22
- Expected to finish
- 2029-07-01
- Last updated by the study team
- 2026-07-17
Who can join
Age: 18 and older, up to 80. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Patients who have mild to moderate corneal endothelial decompensation or bullous keratopathy, but with minimal corneal stromal scarring resulting from irreversible post-surgical corneal decompensation, specifically, all forms of pseudophakic or aphakic bullous keratopathy.
You may not qualify if…
- Severe forms or late-stage presentation of corneal decompensation with severe corneal stromal scarring and or scarring to the DM, unsuitable for SNEC-I.
- Patients with complex anterior segment complications precluding a successful SNEC-I procedure
- Patients who have other forms of endothelial dystrophy, traumatic corneal decompensation, or post-inflammatory corneal decompensation
- Post-laser iridotomy or glaucoma related corneal decompensation
- Patients not keen to participate in the clinical trial
- Patients who are below 21 years of age or above 80 years of age
- Patients who are pregnant
- Patients who are cognitively impaired
- Patients who are prisoners
- Patients with antibiotics/antimycotics allergies
Where it is running
- L V Prasad Eye Institute — Hyderabad, Telangana, India (enrolling)
Full record on ClinicalTrials.gov
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