Methods, systems and devices for treating glaucoma

1. A system for the treatment of ocular pressure comprising:

a needle device including a needle body having a sharp distal end and a proximal end, the needle device configured to form a needle tract in ocular tissue; and

a drainage device including an elongate tube having a length between opposed first and second ends, the elongate tube defining a lumen therethrough, the first end of the tube being directly attached to the proximal end of the needle body, and the elongate tube being configured to move through the needle tract formed by the needle device,

wherein the tube has a plurality of anchor sections spaced from one another along the length of the tube, each anchor section being an enlarged portion of the tube having an outer diameter that is larger than a maximum diameter of the needle body, and wherein at least two anchor sections are spaced by an intermediate section of the tube, the intermediate section having an outer diameter that is smaller than the outer diameters of the at least two anchor sections and wherein the outer diameter of the intermediate section is larger than the maximum diameter of the needle body,

wherein the tube is configurable from a first configuration in which the tube has a natural length with the outer diameter, to a second configuration in which the tube is elongated in length with a reduced outer diameter when the tube is subjected to pulling forces pulling the tube through the needle tract and is subject to resistance forces exerted on the tube by the tissue tract, and

wherein the tube is reconfigurable from the second configuration to the first configuration when the tube is not subjected to the pulling forces and the resistance forces.

2. A system according to claim 1 , wherein:

the proximal end of the needle body defines a cavity that receives the first end of the tube.

3. A system according to claim 2 , wherein:

adhesive bonds the proximal end of the needle body to the first end of the tube disposed in the cavity of the needle body.

4. A system according to claim 2 , wherein:

the proximal end of the needle body surrounds the first end of the tube.

5. A system according to claim 1 , wherein:

the needle body has the following characteristics:

a straight configuration or curved configuration, and

a gauge that is between 30G and 22G.

6. A system according to claim 1 , wherein:

the drainage device is configured to drain aqueous humor from the eye through the lumen of the tube.

7. A system according to claim 6 , wherein

at least one anchor section at least partially remains in the anterior chamber of the eye after implantation of the drainage device into the eye.

8. A system according to claim 1 , wherein:

the drainage device further includes a visual indicator that indicates a proper place where the tube should be cut or otherwise trimmed.

9. A system according to claim 1 , wherein:

the drainage device is formed from a synthetic thermoplastic polymer.

10. A system according to claim 1 , wherein:

the tube is operably coupled to a proximal end of the needle body by at least one of an adhesive, a swaged fitting, a crimping, a whipping, a suture or combinations thereof.

11. A system according to claim 1 , wherein:

the tube is operably coupled to a proximal end of the needle body by an abrupt transition or tapered transition.

12. A system according to claim 1 , wherein:

the material of the tube is configured to allow cutting to decouple the tube from the needle.

13. A system according to claim 1 , wherein:

the lumen extends from the first end of the tube to the second end of the tube.

14. A system for the treatment of ocular pressure comprising:

a needle device including a needle body having a sharp distal end and a proximal end, the needle device configured to form a needle tract in ocular tissue; and

a drainage device including an elongate tube having a length between opposed first and second ends, the elongate tube defining a lumen therethrough, the first end of the tube being directly attached to the proximal end of the needle body, and the elongate tube being configured to move through the needle tract formed by the needle device,

wherein the tube has a plurality of enlarged portions spaced from one another along the length of the tube, wherein each enlarged portion of the tube has an outer diameter that is larger than a maximum diameter of the needle body, the enlarged portion being spaced from the first end of the drainage device, wherein at least two of the enlarged portions are spaced apart by an intermediate portion of the tube, the intermediate portion having an outer diameter that is smaller than the outer diameters of the at least two enlarged portions, and wherein the outer diameter of the intermediate portion is larger than the maximum diameter of the needle body,

wherein the tube is configurable from a first configuration in which the tube has a natural length with the outer diameter, to a second configuration in which the tube is elongated in length with a reduced outer diameter when the tube is subjected to pulling forces pulling the tube through the needle tract and is subject to resistance forces exerted on the tube by the tissue tract, and

wherein the tube is reconfigurable from the second configuration to the first configuration when the tube is not subjected to the pulling forces and the resistance forces,

wherein

the tube is flexible and formed from an elastomeric polymer material, and

the tube has an outer diameter that is between 100 μm and 600 μm.

15. A system according to claim 14 , wherein:

at least one enlarged portion is bulbous in shape.

16. A system according to claim 14 , wherein:

the at least two enlarged portions are configured to fixate the drainage device in the needle tract created by the needle.

17. A system according to claim 14 , wherein:

a ratio of the outer diameter of the intermediate portion of the tube to the maximum outer diameter of the needle body is in the range of 1.25 to 1.8.