Hydrus Microstent and Lens Extraction for the Treatment of Primary Angle-Closure Glaucoma

The objective of this study is to assess the effectiveness of the Hydrus Microstent for lowering intraocular pressure in patients with PAC or PACG. The addition of the Hydrus is expected to lower IOP and medication dependency, and thus reduce the risk of progression of glaucoma. The PCS group will provide a control group to assess the magnitude of the Hydrus treatment effect on IOP, medications, and safety.

Upon successfully meeting the study inclusion/exclusion criteria at both the screening and baseline visits, the subject will be scheduled for surgery. Follow up will be continued for 1 year post surgery, and will include assessments of the subject's IOP, ocular health, and visual acuity status. Visits will be conducted at 1, 7, 30, 90, 180, and 365 days.

A 20% drop in IOP in response to therapy is considered clinically meaningful. The study treatment will be considered successful if a patient can obtain this response in IOP using the same or a fewer number of medications as pre-operative baseline.

Inclusion criteria

Pre-Operative Inclusion Criteria

• Male and Female patients at least 40 years of age.
• An operable age-related cataract with visual impairment or glare, eligible for phacoemulsification.
• Subjects with diagnosed primary angle-closure (PAC; defined as appositional or synechial irido-trabecular contact of 90 degrees or more on gonionscopy) OR primary angle-closure glaucoma (PACG; defined as PAC with documented glaucomatous optic neuropathy and/or reproducible glaucomatous visual field defect), and on > or = 1 glaucoma medication with IOP > or = 21mmHg at both preoperative visits.
• PAC or PACG subjects that are newly diagnosed, or unmedicated (newly diagnosed or non-compliant patient not using medication for > 30 days), with IOP > or = 24mmHg at both preoperative visits.

The subject is able to understand the requirements of the study and is willing to provide written informed consent, follow study instructions, and comply with all study procedures.

Intraoperative Inclusion Critera

• An intact and centered capsulorhexis.
• An intact posterior capsular bag.
• A well-centered IOL implant placed in the capsular bag.
• A clear view and visualization of the angle with direct gonioscopy.
• No evidence of zonular dehiscence/rupture (uncomplicated cataract extraction)

Exclusion criteria

• Pseudophakia in the intended study eye
• All forms of glaucoma other than primary angle-closure (i.e. all open-angle glaucoma including primary open-angle, pseudoexfoliative, or pigmentary glaucoma; neovascular, uveitic, traumatic, steroid induced, lens induced, or glaucoma associated with increased episcleral venous pressure; congenital or developmental glaucoma).
• Secondary angle-closure glaucoma
• Advanced glaucoma, defined as visual field mean deviation worse than -15 dB, or cup-to-disc ration > or = 0.9.
• Visual field depression within the central 5 degrees of fixation, on pattern deviation probability plot.
• Eyes with an anticipated need for incisional glaucoma surgery (e.g. trabeculectomy or tube shunt) within the 12-month follow-up period.
• Central corneal thickness >620 or <490 microns.
• Axial length < or = 19 mm (nanophthalmos).
• Previous incisional glaucoma surgery in the study eye, including trabeculectomy, tube shunt, and non-penetrating procedures such as deep sclerectomy, viscocanalostomy or canaloplasty.
• Plateau iris syndrome.
• History of complicated intraocular surgery.
• Previous MIGS surgery in the study eye.
• Proliferative diabetic retinopathy.
• Previous surgery for retinal detachment.
• Clinically significant corneal dystrophy (e.g. Fuch's Dystrophy).
• Best-corrected visual acuity in the fellow eye worse than 20/200.
• Previous corneal surgery.
• Previous refractive surgery.
• Degenerative visual disorders such as exudative age-related macular degeneration.
• Clinically significant ocular inflammation or infection within thirty days prior to screening.
• Uncontrolled systemic disease that in the opinion of the investigator would put the subject's health at risk and/or prevent the subject from completing all study visits.
• Pregnant or nursing females.