A method for treating advanced primary angle-closure glaucoma (PACG) with cataract includes the steps of: S1, utilizing phacoemulsification cataract extraction combined with intraocular lens implantation (PEI) to remove pupillary block and shallow anterior chamber and reduce a risk of progressive formation of peripheral anterior synechia (PAS); S2, utilizing goinosynchialysis (GSL) to separate the physical adhesion of PAS in the anterior chamber angle with the assistance of a gonioscope and a chopper; and S3, utilizing goniotomy (GT) to incise a dysfunctional trabecular meshwork and a Schlemm canal, so as to remove a dysfunctional trabecular meshwork, enhance outflow of aqueous humor, and reduce intraocular pressure.

A method and delivery system are disclosed for creating an aqueous flow pathway in the trabecular meshwork, juxtacanalicular trabecular meshwork and Schlemm's canal of an eye for reducing elevated intraocular pressure. Pulsed laser radiation is delivered from the distal end of a fiber-optic probe sufficient to cause photoablation of selected portions of the trabecular meshwork, the juxtacanalicular trabecular meshwork and an inner wall of Schlemm's canal in the target site. The fiber-optic probe may be advanced so as to create an aperture in the inner wall of Schlemm's canal in which fluid from the anterior chamber of the eye flows. The method and delivery system may further be used on any tissue types in the body.

A dual blade device and method useable for performing an ab interno procedure within a human eye to remove a strip of trabecular meshwork tissue.

Assemblies and methods for modifying an intraocular pressure of a patient's one or both eyes are disclosed. The assemblies and methods can be used to treat, inhibit, or prevent ocular conditions such as glaucoma, high intraocular pressure, optic disc edema, idiopathic intracranial hypertension, zero-gravity induced papilledema, and other optic pressure related conditions. An assembly can include a goggle including at least one cavity, a pump in fluid communication with the at least one cavity, and a control mechanism. The control mechanism can be operatively coupled to the pump and can maintain a target pressure or target pressure range in the at least one cavity, which, when the assembly is worn by a patient, is the area between a patient's eye(s) and wall surfaces of the goggle. Controlling the pressure over the outer surfaces of the patient's eye(s) can drive a desired change in the intraocular pressure of the eye(s).

Devices, methods and kits are described for reducing intraocular pressure. The devices include a support that is implantable within Schlemm's canal and maintains the patency of the canal without substantially interfering with transmural fluid flow across the canal. The devices utilize the natural drainage process of the eye and can be implanted with minimal trauma to the eye. Kits include a support and an introducer for implanting the support within Schlemm's canal. Methods include implanting a support within Schlemm's canal, wherein the support is capable of maintaining the patency of the canal without substantial interference with transmural fluid flow across the canal.

Apparatus and methods for ocular treatment are provided. The apparatus can comprise an outer sheath and a microcannula movably housed within the outer sheath and having a proximal end, a distal end, a cavity, and a central longitudinal axis. The apparatus can include a first protrusion extending circumferentially inward at a distal end of the outer sheath and a second protrusion located on an outer circumferential surface of the microcannula. The apparatus can include multiple orifices disposed on the microcannula distal end, each of the orifices defining a channel extending transverse to the central longitudinal axis and configured to deliver a substance radially outwardly from the distal tip of the microcannula. The distal tip can extend out from a distal opening of the outer sheath when the microcannula is in an extended position and can be housed within the outer sheath when the microcannula is in a retracted position.

Devices and methods to remove trabecular meshwork to treat glaucoma and other conditions which may not utilize cutting elements when stripping the trabecular meshwork. The trabeculorhexis parts tissue by applying non-cutting shear and tension to the tissue to disinsert the tissue from its attachments. Reducing or eliminating the need for sharp cutting implements in the eye reduces the likelihood of incisional bleeding, iris and scleral tissue maceration and further inadvertent tissue damage of the gonio structure of the eye. In another aspect, a cutting element may be used to form a circumferential slit in a wall of Schlemm's canal in conjunction with removal of trabecular meshwork or independently.

A surgical instrument (1) is provided with a rigid probe (2), and cuts off the trabecular meshwork by inserting this probe (2) into the canal of Schlemm. An inner tube portion having a cutter is equipped inside the probe, and the trabecular meshwork sucked in from a hole portion (22) is cut off by the cutter due to the movement of the inner tube portion. A protection portion (21) is formed on the tip the probe (2) and protects the outer wall of the canal of Schlemm when cutting the trabecular meshwork. According to the invention, an ophthalmic surgical instrument for glaucoma patients is provided, the surgical instrument having excellent operability and preventing cutting of parts that should not be cut off without fail.

An ocular implant including an intraocular pressure sensor and having an inlet portion and a Schlemm's canal portion distal to the inlet portion, the inlet portion being disposed at a proximal end of the implant and sized and configured to be placed within an anterior chamber of a human eye, the Schlemm's canal portion being arranged and configured to be disposed within Schlemm's canal of the eye when the inlet portion is disposed in the anterior chamber.

An ophthalmological device (10) for the treatment of corneal diseases such as keratocanus and glaucoma, comprises a molding head (12), a suction body (14) and a UV lamp (15). The molding head (12) has a hollow cylindrical configuration and includes a rigid molding lens (18) for shaping the cornea of an eye (11) of a patient. The lens is curved and defines a plurality of apertures therein. The suction body (14) has a hollow cylindrical configuration. The lamp (15) is fitted to the suction body. Molding head (12) and suction body (14) together define a chamber (32) from which air is evacuated so as to induce a partial vacuum within the chamber (32) for attracting the cornea onto the lens (18). A photo-sensitizer is applied to the eye and while the cornea is held against the mold, it is irradiated with UV light by lamp (15) so as to cross-link collagen fibers in the cornea.