Bipolar radiofrequency ablation systems for treatment within bone
System and methods for channeling a path into bone include a trocar having a proximal end, distal end and a central channel disposed along a central axis of the trocar. The trocar includes a distal opening at the distal end of the trocar. The system includes a curved cannula sized to be received in the central channel, the curved cannula comprising a curved distal end configured to be extended outward from the distal opening to generate a curved path extending away from the trocar. The curved cannula has a central passageway having a diameter configured to allow a treatment device to be delivered through the central passageway to a location beyond the curved path.
1. A system for navigating to and providing treatment within bone, the system comprising:
an introducer having a central channel and an opening at a distal tip of the introducer;
a first stylet configured to be installed in the introducer, the first stylet comprising a sharp distal tip that is configured to extend beyond the opening at the distal tip of the introducer and to pierce an outer cortical bone region of the bone;
a channeling instrument configured to be inserted through the introducer after removal of the first stylet to create a predetermined-length linear path within a cancellous region of the bone toward a target treatment site;
a cannula configured to be inserted through the introducer after removal of the first stylet, the cannula having a deflectable distal tip configured to form a curved path within the bone;
a second stylet configured to be installed within a central passageway of the cannula and to extend beyond an opening at a distal end of the central passageway,
wherein the second stylet and the cannula together form the curved path within the bone; and
a bipolar radiofrequency probe configured to be inserted through the introducer after removal of the channeling instrument or the second stylet, the bipolar radiofrequency probe being configured to deliver radiofrequency energy sufficient to ablate a basivertebral nerve at the target treatment site within the bone,
wherein the bipolar radiofrequency probe comprises a sensor.
2. The system of claim 1 , wherein:
the first stylet is straight;
the bipolar radiofrequency probe comprises two spaced-apart electrodes; and
the introducer and the first stylet are configured to percutaneously access the bone.
3. The system of claim 1 , wherein the bone is a lumbar vertebral body or an S1 vertebral body.
4. The system of claim 1 ,
wherein the cannula comprises a locking nut configured to engage with the introducer to stop additional advancement.
5. The system of claim 1 , wherein the system is configured to treat multiple vertebrae.
6. A system for navigating to and providing treatment within bone, the system comprising:
a trocar having a central channel and an opening at a distal tip of the trocar;
a first stylet configured to be installed in the trocar, the first stylet comprising a sharp distal tip that is configured to extend beyond the opening at the distal tip of the trocar and to pierce an outer cortical bone region of the bone;
a channeling instrument configured to be inserted through the trocar after removal of the first stylet to create a predetermined-length linear path within a cancellous region of the bone toward a target treatment site;
a cannula configured to be inserted through the trocar after removal of the first stylet, the cannula having a deflectable distal tip configured to form a curved path within the bone;
a second stylet configured to be installed within a central passageway of the cannula and to extend beyond an opening at a distal end of the central passageway,
wherein the second stylet and the cannula together form the curved path within the bone; and
a treatment device configured to be inserted through the trocar and deliver radiofrequency energy sufficient to ablate a basivertebral nerve at the target treatment site,
wherein the bone is a lumbar vertebral body or an Si vertebral body; and
a sensor configured to perform measurements at the treatment site.
7. The system of claim 6 , wherein:
the first stylet is straight;
the treatment device comprises a bipolar radiofrequency probe that comprises two spaced-apart electrodes; and
the trocar and the first stylet are configured to percutaneously access the bone.
8. The system of claim 6 , wherein the sensor is positioned on a distal tip of a separate probe.
9. The system of claim 6 , wherein the system is configured to treat multiple vertebrae.
10. The system of claim 6 , wherein the cannula comprises a locking nut configured to engage with the trocar to stop additional advancement of the cannula.
11. The system of claim 6 , wherein the cannula comprises a tube having a pattern of relief or cuts in a wall of the tube.
12. The system of claim 6 , wherein the treatment device comprises two spaced-apart electrodes.
13. The system of claim 6 , wherein the deflectable distal tip of the cannula has a preformed curvature, and wherein the second stylet comprises a distal end portion having a preformed curvature corresponding to the preformed curvature of the deflectable distal tip of the cannula.