RE-SHAPING INTRAGASTRIC IMPLANTS

• US 20120089172A1
• Filed: 10/10/2011
• Published: 04/12/2012
• Est. Priority Date: 10/11/2010
• Status: Abandoned Application

• Current Assignee: Allergan, Inc. (Canada) (Abbvie Incorporated)
• Original Assignee: Allergan, Inc. (Canada) (Abbvie Incorporated)
• Inventors: Dominguez, Zachary, Raven, Joseph S., Babkes, Mitchell H., Mudd, Christopher S.
• Application Number:
  US13/270,016
• Publication Number:
  US 20120089172A1
• Time in Patent Office: Days
• US Class Current: 606/192
• CPC Class Codes: A61F 5/0036 Intragastrical devices

Abstract

The present application provides implantable intragastric devices for the treatment of obesity. The intragastric devices advantageously act as a volume-occupying device, and is able to survive implantation in a patient'"'"'s stomach for a year or longer. In addition, the intragastric devices may be configured to stimulate an inner stomach wall and/or temporarily block the pylorus to slow gastric emptying and/or be rotationally variant, thereby encouraging different stimulation points on the inner wall of the stomach and limiting the stomach'"'"'s ability to adapt over long term implantation. The intragastric devices may reshape the stomach cavity, such as by pushing on opposite sides so as to “planarize” the stomach. For instance, the device may be an inflated disk, or an implantable loop or a springy coil that may be straightened for delivery/extraction yet assume the loop or coil shape upon implant.

Claims

1. An intragastric obesity treatment implant that stimulates the stomach walls, comprising:

an inflatable member having an inflated size that will not pass through the pyloric sphincter and a volume within the stomach of at least 400 ml and being made of a material that will resist degradation over a period of at least six months within the stomach, the inflatable member being formed as a substantially planar disc having opposed faces and a peripheral surface and a maximum width larger than the contracted width of an adult stomach so alter the shape of the stomach to conform somewhat to the inflatable member,

the implant being formed of a material which permits it to be compressed when deflated into a substantially linear delivery configuration.

2. The implant of claim 1, further including a plurality of dimples on each opposed face of the substantially planar disc defining points at which the opposed faces are connected through an inner cavity to help retain the substantially planar disc shape.

3. The implant of claim 1, wherein the opposed faces and peripheral surface are smooth.

4. The implant of claim 1, wherein the opposed faces are generally circular with a diameter, and the peripheral surface defines a thickness that is less than one-half the diameter.

5. The implant of claim 1, at least some of the opposed faces and peripheral surface are irregular in a pattern selected from the group consisting of a rounded protrusion, a quill-like extension, a recess, and combinations thereof.

6. The implant of claim 1, wherein the intragastric device is constructed out of a material selected from a group consisting of a rubber, a fluorosilicone, a fluoroelastomer, a thermoplastic elastomer, and combinations thereof.

7. An intragastric obesity treatment implant that stimulates the stomach walls, comprising:

an elongated member having a relaxed configuration that forms a coil, opposite free ends of the coil overlapping one another to permit constriction of the coil, the coil having a diameter that generally fits within the stomach of an adult patient so as to contact the interior stomach walls upon contraction thereof, the elongated member being formed of a material which permits it to be stretched into a substantially linear delivery configuration and that will resist degradation over a period of at least six months within the stomach.

8. The implant of claim 7, wherein the coil in its relaxed configuration has a diameter of between about 15-16 cm.

9. The implant of claim 7, wherein the coil comprises an inner pre-formed wire placed inside a soft and fairly flexible plastic tubular sheath.

10. The implant of claim 9, wherein the wire is Nitinol.

11. The implant of claim 9, wherein two free ends of the wire are captured by two end caps that close open ends of the sheath.

12. The implant of claim 11, wherein the assembled components of the wire, sheath and end caps are preferably coated with a flexible compound that is resistant to stomach juices.

13. The implant of claim 9, wherein the wire is embedded within the sheath with no hollow spaces therebetween.

14. An intragastric obesity treatment implant that stimulates the stomach walls, comprising:

an elongated hollow member having a relaxed configuration that forms a loop, opposite free ends of the loop being adapted to connect together, the loop having a diameter that generally fits within the stomach of an adult patient so as to contact the interior stomach walls upon contraction thereof, the elongated hollow member being formed of a material which permits it to be stretched into a substantially linear delivery configuration and that will resist degradation over a period of at least six months within the stomach.

15. The implant of claim 14, wherein the elongated hollow member further including perforations along its length to permit ingress of stomach fluids.

16. The implant of claim 14, wherein the elongated hollow member has a distal end connector with a lumen, and a proximal end connector with a lumen and a side aperture spaced from the proximal end connector, the implant further including a tether that extends through the hollow lumen on the distal end connector and is secured therein, and passes in through the proximal end connector lumen and outward through the side aperture, the proximal and distal end connectors being brought together upon pulling the tether taut.

17. The implant of claim 14, wherein the loop has a diameter of between about 15-16 cm.

18. The implant of claim 14, further including a spring placed inside the elongated hollow member to provide resiliency and prevent kinking of the elongated hollow member.

19. The implant of claim 14, wherein the loop is constructed by cutting a plastic tube in two to form two smaller diameter half tubes that fit inside a larger diameter whole tube.