Table 3.
References | PN | Design | Target | Indication | FU | Outcome | SAE/AE |
---|---|---|---|---|---|---|---|
Non-invasive lesioning (non-reversible) | |||||||
Gallay et al. [67] | 8 | PT | MRgFUS | TN | 53 months | Mean pain relief 3 months: 51% | None |
Posterior part of the central lateral thalamic nucleus (peak 51–64 °C) | Mean pain relief 12 months: 71% | ||||||
Mean pain relief 53 months: 78% | |||||||
Jeanmonod et al. [66] | 12 | PT | MRgFUS | NP | 12 months | Mean pain relief 3 months: 49% | 1 ICH |
Posterior part of the central lateral thalamic nucleus (peak 51–64 °C) | Mean pain relief 12 months: 57% | ||||||
Gallay et al. [65] | 180 (treatments) | PT | MRgFUS | NP | 3 months | Not reported | None |
Posterior part of the central lateral thalamic nucleus (peak 51–64 °C) | |||||||
Martin et al. [64] | 9 | PT | MRgFUS | NP | NA | Mean pain relief after 2 days: 68% | None |
VPL (peak temperature 51–60 °C) |
MRgFUS magnet resonance guided focused ultrasound, PT pilot study, RCT randomized controlled trial, CR case report, VPL nucleus ventrolateralis of the thalamus, CPSP chronic post-stroke pain, FU follow-up, SAE/AE serious adverse event, ICH intracranial haemorrhage, NP neuropathic pain, TN trigeminal neuralgia, NA not applicable