Systems and methods for therapeutic nasal neuromodulation
The invention generally relates to systems and methods for therapeutically modulating nerves in or associated with a nasal region of a patient for the treatment of a rhinosinusitis condition.
1. A device for treating a condition within a nasal cavity of a patient, the device comprising:
a shaft and a multi-segment end effector operably coupled thereto, the multi-segment end effector is configured for delivering energy to one or more target sites within the nasal cavity of the patient, the multi-segment end effector comprises a proximal segment and a separate distal segment spaced apart from the proximal segment and each of the proximal and distal segments is transformable between a retracted configuration and an expanded deployed configuration;
wherein the proximal segment comprises:
a first pair of flexible support elements each comprising one or more energy delivering elements arranged thereon, the first pair of flexible support elements extend in a first outward direction relative to a longitudinal axis along which the shaft lies and cooperatively form an inwardly extending first concave shape relative to the longitudinal axis when the first segment is in the expanded deployed configuration; and
a second pair of flexible support elements each comprising one or more energy delivering elements arranged thereon, the second pair of flexible support elements extend in a second outward direction relative to the longitudinal axis and opposing the first outward direction and cooperatively form an inwardly extending second concave shape relative to the longitudinal axis and opposing the first concave shape when the first segment is in the expanded deployed configuration.
2. The device of claim 1 , wherein:
the one or more energy delivering elements arranged on the first and second pairs of flexible support elements are configured to deliver energy to tissue at a first target site; and
the distal segment comprises a set of flexible support elements each comprising one or more energy delivering elements arranged thereon and configured to deliver energy to tissue at a second target site.
3. The device of claim 2 , wherein each of the proximal and distal segments is configured to position one or more of the respective energy delivering elements at the first and second target sites when in the deployed configuration.
4. The device of claim 2 , wherein, when the distal segment is in the expanded deployed configuration, each of the set of flexible support elements extend in an outward direction relative to the longitudinal axis to cooperatively form an open-ended circumferential shape.
5. The device of claim 1 , wherein the first and second pairs of flexible support elements of the proximal segment comprise deformable composite wires.
6. The device of claim 5 , wherein the composite wires comprise shape memory material.
7. The device of claim 1 , wherein the one or more energy delivering elements comprise electrodes configured to deliver radiofrequency (RF) energy to tissue at respective target sites within the nasal cavity, wherein the respective target sites are associated with parasympathetic nerve supply.
8. The device of claim 7 , wherein the electrodes are configured to deliver RF energy at a level sufficient to therapeutically modulate postganglionic parasympathetic nerves innervating nasal mucosa at an innervation pathway within the nasal cavity of the patient.
9. The device of claim 8 , wherein the condition is selected from the group consisting of allergic rhinitis, non-allergic rhinitis, chronic rhinitis, acute rhinitis, chronic sinusitis, acute sinusitis, chronic rhinosinusitis, acute rhinosinusitis, and medical resistant rhinitis.
10. A method for treating a condition within a nasal cavity of a patient, the method comprising:
advancing a device comprising a shaft and a multi-segment end effector operably coupled thereto, the multi-segment end effector is configured for delivering energy to one or more target sites within the nasal cavity of the patient, the multi-segment end effector comprising a proximal segment and a separate distal segment spaced apart from the distal segment and each of the proximal and distal segments is transformable between a retracted configuration and an expanded deployed configuration, wherein the proximal segment comprises:
a first pair of flexible support elements each comprising one or more energy delivering elements arranged thereon, the first pair of flexible support elements extend in a first outward direction relative to a longitudinal axis along which the shaft lies and cooperatively form an inwardly extending first concave shape relative to the longitudinal axis when the first segment is in the expanded deployed configuration; and
a second pair of flexible support elements each comprising one or more energy delivering elements arranged thereon, the second pair of flexible support elements extend in a second outward direction relative to the longitudinal axis and opposing the first outward direction and cooperatively form an inwardly extending second concave shape relative to the longitudinal axis and opposing the first concave shape when the first segment is in the expanded deployed configuration;
deploying the proximal segment at a first target site within the nasal cavity; and
delivering energy, via the one or more energy delivering elements arranged on at least one of the first and second pairs of flexible support elements, to tissue at the first target site.
11. The method of claim 10 , wherein:
the one or more energy delivering elements arranged on the first and second pairs of flexible support elements are configured to deliver energy to tissue at the first target site; and
the distal segment comprises a set of flexible support elements each comprising one or more energy delivering elements arranged thereon and configured to deliver energy to tissue at a second target site.
12. The method of claim 11 , wherein each of the proximal and distal segments is configured to position one or more of the respective energy delivering elements at the first and second target sites when in the deployed configuration.
13. The method of claim 11 , wherein, when the distal segment is in the expanded deployed configuration, each of the set of flexible support elements extend in an outward direction relative to the longitudinal axis to cooperatively form an open-ended circumferential shape.
14. The method of claim 10 , wherein the first and second pairs of flexible support elements of the proximal segment comprise deformable composite wires.
15. The method of claim 14 , wherein the composite wires comprise shape memory material.
16. The method of claim 11 , further comprising deploying the distal segment of the multi-segment end effector at the second target site to thereby position one or more of the set of energy delivering elements at the second target site.
17. The method of claim 16 , wherein the one or more energy delivering elements comprise electrodes, wherein delivering energy via the proximal and distal segments comprises delivering radiofrequency (RF) energy, via one or more of the electrodes, at a level sufficient to therapeutically modulate postganglionic parasympathetic nerves innervating nasal mucosa at an innervation pathway within the nasal cavity of the patient.
18. The method of claim 17 , wherein the condition is selected from the group consisting of allergic rhinitis, non-allergic rhinitis, chronic rhinitis, acute rhinitis, chronic sinusitis, acute sinusitis, chronic rhinosinusitis, acute rhinosinusitis, and medical resistant rhinitis.