Clot retrieval device for removing clot from a blood vessel
A clot removal device for removing clot from a body vessel includes an expandable structure having a constrained delivery configuration, an expanded clot engaging deployed configuration, and an at least partially constrained clot pinching configuration, the expandable structure including a proximal section comprising a plurality of struts with opening angles; a mid-section distal of the proximal section and comprising a plurality of struts with opening angles and cells larger than cells of the proximal section, the mid-section being configured to expand a larger radial extent in the deployed configuration than the proximal section to provide clot grip and retention during retraction of the clot; wherein the proximal section is configured to pinch the clot from the body vessel when partially resheathed by a microcatheter.
1. A clot removal device for removing a clot from a body vessel, comprising:
an expandable structure having a constrained delivery configuration, an expanded clot engaging deployed configuration, and an at least partially constrained clot pinching configuration, the expandable structure comprising:
a proximal section comprising:
a plurality of struts with opening angles and cells; and
alternating clot embedding cells and segments of lower outward radial force;
a mid-section distal of the proximal section and comprising a plurality of struts with opening angles and cells larger than the cells of the proximal section, the mid-section being configured to expand to a larger radial extent in the deployed configuration than the proximal section to provide clot grip and retention during retraction of the clot;
wherein the proximal section is configured to pinch the clot from the body vessel when partially resheathed by a microcatheter.
2. The device of claim 1 , wherein the proximal section is configured to pinch the clot located in and/or between cells of the proximal section as the device is moved from the expanded deployed configuration to the at least partially constrained clot pinching configuration.
3. The device of claim 1 , wherein a radial force exerted by the clot embedding cells and segments of lower outward radial force differ from each other.
4. The device of claim 1 , wherein a size of the clot embedding cells of the proximal section is smaller than the segments of lower outward radial force.
5. The device of claim 1 , wherein in the deployed configuration, a ratio of a diameter of the mid-section to a diameter of the proximal section diameter ranges between 1.5:1 to 4:1.
6. The device of claim 1 , wherein in the deployed configuration, a ratio of a diameter of the mid-section to a diameter of the proximal section diameter ranges between 2:1 and 3:1.
7. The device of claim 1 , wherein the proximal section comprises a fixed deployment diameter of approximately about 1 mm.
8. The device of claim 1 , wherein the device comprises a radiopaque marker at a transition between the proximal section and the mid-section.
9. The device of claim 1 , wherein the proximal section and the mid-section comprise different strut lengths causing a radial force profile of the proximal section to be different than a radial force profile of the mid-section.
10. The device of claim 1 , wherein the proximal section and the mid-section comprise different patterns causing a radial force profile of the proximal section to be different than a radial force profile of the mid-section.
11. A clot removal device for removing a clot from a body vessel, comprising:
an expandable structure having a constrained delivery configuration, an expanded clot engaging deployed configuration, and an at least partially constrained clot pinching configuration, the expandable structure comprising:
a proximal section comprising a plurality of struts with opening angles and cells;
a mid-section distal of the proximal section and comprising a plurality of struts with opening angles and cells larger than cells of the proximal section, the mid-section being configured to expand to a larger radial extent in the deployed configuration than the proximal section to provide clot grip and retention during retraction of the clot;
wherein the proximal section is configured to pinch the clot from the body vessel when partially resheathed by a microcatheter, wherein the proximal section and the mid-section comprise different strut lengths causing a radial force profile of the proximal section to be different than a radial force profile of the mid-section.
12. The device of claim 11 , wherein the proximal section and the mid-section comprise different strut lengths causing a radial force profile of the proximal section to be less than a radial force profile of the mid-section.
13. The device of claim 11 , wherein the proximal section and the mid-section comprise different patterns causing a radial force profile of the proximal section to be greater than a radial force profile of the mid-section.
14. The device of claim 11 , wherein the proximal section and the mid-section comprise different patterns causing a radial force profile of the proximal section to be less than a radial force profile of the mid-section.
15. The device of claim 11 , wherein the proximal section and the mid-section comprise different strut lengths causing a radial force profile of the proximal section to be greater than a radial force profile of the mid-section.
16. A system for removing a clot from a vessel, comprising:
a microcatheter; and
a clot removal device removably inserted in a lumen of the microcatheter, comprising:
an expandable structure having a constrained delivery configuration within the lumen, an expanded clot engaging deployed configuration when distal of the microcatheter, and an at least partially constrained clot pinching configuration, the expandable structure comprising:
a proximal section comprising:
a plurality of struts with opening angles and cells; and
alternating clot embedding cells and segments of lower outward radial force; and
a mid-section distal of the proximal section and comprising a plurality of struts with opening angles and cells larger than the cells of the proximal section, the mid-section being configured to expand a larger radial extent in the deployed configuration than the proximal section to provide clot grip and retention during retraction of the clot;
wherein the proximal section is configured to pinch the clot from the body vessel when partially resheathed by the microcatheter.
17. The system of claim 16 , wherein the proximal section is configured to pinch the clot located in and/or between the cells of the proximal section as the device is moved from the expanded deployed configuration distal of the microcatheter to the at least partially constrained clot pinching configuration.
18. The device of claim 16 , wherein a size of the clot embedding cell of the proximal section is smaller than the segments of lower outward radial force.
19. The system of claim 16 , wherein the proximal section and the mid-section comprise different strut lengths causing a radial force profile of the proximal section to be greater than a radial force profile of the mid-section.
20. The system of claim 16 , wherein portions between the cells of the proximal section are configured to deliver relatively low radial force to the vessel with minimized surface contact area between struts of the proximal section and the clot.
21. The system of claim 16 , wherein the device comprises a radiopaque marker at a transition between the proximal section and the mid-section.