2020
DOI: 10.1016/j.neulet.2020.134760
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Time-course of pain threshold after continuous theta burst stimulation of primary somatosensory cortex in pain-free subjects

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Cited by 10 publications
(2 citation statements)
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“…After their inclusion, participants were randomly assigned to one of two groups: (1) SRPS and (2) No SRPS. In spite of their group allocation, each participant took part in two single-day laboratory visits, one with active rTMS and the other with a sham intervention, separated by at least 1 week to avoid any potential carry-over effects of the first visit on the other ( 22 , 47 , 48 ). Each visit included two consecutive sessions of rTMS (or sham) spaced 10 min apart ( Figure 1 ).…”
Section: Methodsmentioning
confidence: 99%
“…After their inclusion, participants were randomly assigned to one of two groups: (1) SRPS and (2) No SRPS. In spite of their group allocation, each participant took part in two single-day laboratory visits, one with active rTMS and the other with a sham intervention, separated by at least 1 week to avoid any potential carry-over effects of the first visit on the other ( 22 , 47 , 48 ). Each visit included two consecutive sessions of rTMS (or sham) spaced 10 min apart ( Figure 1 ).…”
Section: Methodsmentioning
confidence: 99%
“…These findings support the general consensus that rTMS exerts a multitude of mechanisms that could differentially modulate specific types of pain and indicate an acute analgesic effect that could be independent from the maladaptive plasticity associated with chronic pain. Indeed, rTMS application is shown to activate opioid-mediated analgesia of acute pain in healthy individuals [79], induce dose-dependent immediate analgesia following stimulation in patients with intractable neuropathic pain [80] and elevate electrical pain thresholds up to 40 min following application over the somatosensory cortex of healthy subjects without altering the excitability of the M1 cortex [81]. Therefore, rTMS carries significant potentials in both: prevention of acuteto-chronic pain transition, through acute analgesia and prevention of maladaptive plasticity, and treatment of chronic pain through reversal of maladaptive plasticity.…”
Section: Non-invasive Brain Stimulationmentioning
confidence: 99%