CyPass Clinical Experience Study (CyCLE)

Transcend Medical

Status: Completed

Conditions: Open Angle Glaucoma (OAG)

Treatments: Device: CyPass Micro-Stent

Study type: Observational

Funder types: Industry

Identifiers

NCT01097174

TMI-09-02

Details and patient eligibility

About

This study is to evaluate the long-term safety, effectiveness and clinical experience of the CyPass Micro-Stent in patients with glaucoma.

Enrollment: 555 patients

Sex: All

Volunteers: No Healthy Volunteers

Inclusion criteria

• Diagnosis of OAG
• IOP ≥ 21 mmHg and ≤ 31 mmHg (with or without ocular hypotensive medication)

Exclusion criteria

• Acute angle closure, narrow angle, uveitic or neovascular glaucoma
• Normal tension glaucoma

Trial design

555 participants in 1 patient group

CyPass Micro-stent

Description:

Patients in whom CyPass Micro-stent implantation was attempted.

Treatment:

Device: CyPass Micro-Stent