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Study identifier: NCT01756365 Synced from ClinicalTrials.gov · July 28, 2026
● Recruiting

Autologous Cultured Corneal Epithelium (CECA) for the Treatment of Limbal Stem Cell Deficiency

Condition: Limbal Stem Cell Deficiency  ·  Sponsor: CHU de Quebec-Universite Laval

PhaseNA
Planned participants54
Who can joinAll sexes, 1 Year to no upper limit
Healthy volunteersNo

About this study

The study " Autologous cultured corneal epithelium (CECA) for the treatment of corneal lesions associated with limbal stem cell deficiency" is the first clinical trial of this product manufactured at the LOEX laboratory. The culture of corneal epithelium strives to produce a reconstructed tissue with the therapeutical aim of treatment of limbal stem cell deficiency. The study is a phase I/phase II study with the goal to evaluate safety and efficacy of the CECA graft for the treatment of human patients suffering from limbal stem cell deficiency. The trial is open to all genders. The inclusion of 5 minors is planned.

This description comes directly from the study's public registry record.

Talk to the study team

Contact details are listed per location below or on the registry record.

Always discuss trial participation with your own doctor first.

Locations (4)

University Health Network - Toronto Western HospitalToronto, Ontario, CanadaRecruiting
CIUSSS de l'Est de l'île de MontréalMontreal, Quebec, CanadaRecruiting
McGill University Health Centre; Centre de Médecine Innovatrice/Centre for Innovative MedicineMontreal, Quebec, CanadaRecruiting
Centre universitaire d'Ophtalmologie CHU de Québec - HSSQuébec, Quebec, CanadaRecruiting

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Source record: clinicaltrials.gov/study/NCT01756365