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The objective of this early feasibility clinical study is to evaluate the safety and effectiveness of the GORE Glaucoma Drainage Implant (2 configurations) in subjects with primary open-angle glaucoma that is uncontrolled by hypotensive medications or for which conventional incisional glaucoma surgery would be more likely to fail due to scarring.
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Interventional model
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20 participants in 2 patient groups
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Central trial contact
Kathy Sullivan; Mary Drew
Data sourced from clinicaltrials.gov
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