5 Years Long Term Results After Standalone CyPass-Implantation

Dietrich-Bonhoeffer-Klinikum

Status: Completed

Conditions: Glaucoma

Treatments: Diagnostic Test: Glaucoma diagnostics

Study type: Observational

Funder types: Industry

Identifiers

NCT03114059

STI 06/16

Details and patient eligibility

About

This study evaluates the results of all clinically relevant findings of glaucoma diagnostics 5 Years after stent-implantation concerning the safety and effectiveness of the cypass stent procedure. The comparison of Preoperative and long term postoperative results is the aim of this study to evaluate this young procedure of Glaucoma surgery

Full description

This is a post market study without interventions.The participants have been treated with CyPass-Stent implantation between 3 and 7 years ago to control the intraocular pressure . They will be invited for only one follow up visit to determine the present glaucoma status again, to determine the long term safety and effectiveness of the cypass stent procedure and to see whether addition therapy or surgical intervention is necessary.

Enrollment: 230 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• patients who have undergone a standalone cypass implantation at least 3 years ago
• signed inform consent

Exclusion criteria

• Patients with too much travel distance between study center and home
• Patients who cannot visit the studycenter due to health problems

Trial design

230 participants in 1 patient group

standalone CyPass implantation

Description:

patients who have undergone a standalone cypass implantation without cataract surgery more than 3 years ago

Treatment:

Diagnostic Test: Glaucoma diagnostics