122
Participants
Start Date
November 21, 2023
Primary Completion Date
June 20, 2024
Study Completion Date
June 20, 2024
EX-PRESS P-50 filtration device
FDA-approved, stainless steel device with a 50-micron internal lumen size indicated for the reduction of intraocular pressure in glaucoma patients where medical and conventional surgical treatments have failed
EX-PRESS P-200 filtration device
FDA-approved, stainless steel device with a 200-micron internal lumen size indicated for the reduction of intraocular pressure in glaucoma patients where medical and conventional surgical treatments have failed
Boozman Hoff Regional Eye Clinic, Rogers
El Paso Eye Surgeons, PA, El Paso
Lead Sponsor
Alcon Research
INDUSTRY