NCT03807869

Reduction of Intraocular Pressure After I-stent By-pass Implantation in Eyes With Open Angle Glaucoma

Efficacy and Safety of I-stent By-pass Implantation in Eyes With Open Angle Glaucoma

• Status: Completed
• Phase: N/A
• Study type: Interventional
• Enrollment: 73 (actual)
• Sponsor: Medical University of Bialystok · Academic / Other
• Sex: All
• Age: 18 Years
• Healthy volunteers: Accepted

Summary

Purpose of this study is to exam the hypotensive effectiveness of I-stent implantation depended on number of antiglaucoma eye drops at baseline.

Detailed description

The scientific aim of the project is to estimate the average reduction of intraocular pressure (IOP) in relation to the initial number of antiglaucoma drops at the end of 12 months observation period. The subject must suffer from glaucoma and cataract at the same time, and qualify for a cataract surgery. The group will be composed of 40 patients of the Ophthalmology Clinic of the Medical University of Białystok qualified for planned cataract removal surgery. They will be surgically implanted an I-stent by-pass during phacoemulsification.

Conditions

• Glaucoma

Interventions

Type	Name	Description
PROCEDURE	combined glaucoma surgery	phacoemulsification of cataract and I-stent by-pass implantation

Timeline

• Start date: 2018-12-01
• Primary completion: 2019-12-01
• Completion: 2020-02-01
• First posted: 2019-01-17
• Last updated: 2020-02-13

Locations

1 site across 1 country: Poland