The Role of Transscleral Cyclophotocoagulation in Patients Undergoing a Boston Keratoprosthesis

Recruiting N/A Interventional Study
Glaucoma Eye Diseases Cornea Disease
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 80
Sex
Any
Study type
Interventional
Purpose
Prevention
Participants needed
20 (estimated)
Sponsor
Centre hospitalier de l'Université de Montréal (CHUM) · Other
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About This Trial
The Boston keratoprosthesis (KPro) is a special plastic device that is used to replace a sick cornea (transparent part of the eye, in front of the iris) in order to restore vision in patients who have failed traditional corneal transplants or have a very poor prognosis of success. Glaucoma is a chronic disease which causes optic nerve damage secondary to high pressure inside the eye and could lea…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Adults patients * Able to give an informed consent * Capable of being followed during the study * Candidate for the Boston keratoprosthesis type I Exclusion Criteria: * Patients younger than 18 years old or older than 80 years old * Unable to give an informed consent * Parti…
Contacts

Marie-Catherine Thessier, MSc

514 890-8000

marie-catherine.tessier.chum@ssss.gouv.qc.ca

CONTACT

Soumaya Bouhout, MD

5142640436

soumaya.bouhout@umontreal.ca

CONTACT