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A randomized controlled trial of 5 daily sessions and continuous trial of 4 weekly sessions of repetitive transcranial magnetic stimulation for neuropathic pain

机译:随机对照试验5日每日休会和连续试验4每周一次重复的经颅磁刺激治疗神经病疼痛

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We conducted a multicenter, randomized, patient- and assessor-blinded, sham-controlled trial to investigate the efficacy of repetitive transcranial magnetic stimulation (rTMS) of the primary motor cortex (M1) in patients with neuropathic pain (NP). Patients were randomly assigned to receive 5 daily sessions of active or sham rTMS of M1 corresponding to the part of the body experiencing the worst pain (500 pulses per session at 5 Hz). Responders were invited to enroll in an open-label continuous trial involving 4 weekly sessions of active rTMS. The primary outcome was a mean decrease in a visual analogue scale of pain intensity (scaled 0-100 mm) measured daily during the daily sessions in an intention-to-treat population. Secondary outcomes were other pain scores, quality-of-life measures, and depression score. One hundred forty-four patients were assigned to the active or sham stimulation groups. The primary outcome, mean visual analogue scale decreases, was not significantly different (P = 0.58) between the active stimulation group (mean, 8.0) and the sham group (9.2) during the daily sessions. The secondary outcomes were not significantly different between 2 groups. The patients enrolled in the continuous weekly rTMS achieved more pain relief in the active stimulation group compared with the sham (P < 0.01). No serious adverse events were observed. Five daily sessions of rTMS with stimulus conditions used in this trial were ineffective in short-term pain relief in the whole study population with various NP. Long-term administration to the responders should be investigated for the clinical use of rTMS on NP in the future trials.
机译:我们进行了多中心,随机,患者和评估综合症,假手段试验,以研究初级运动皮层(M1)在神经病疼痛(NP)患者中的重复经颅磁刺激(RTMS)的功效。患者被随机分配接受5日期的M1的活性或假期,对应于体内体验最严重的疼痛(5 Hz的每次500次脉冲)。被邀请响应者注册开放标签的连续试验,涉及4每周有效RTMS会话。主要结果是在日常会话期间每天测量的疼痛强度(缩放0-100mm)的视觉模拟等级的平均降低,以便治疗人口。二次结果是其他疼痛评分,生活质量措施和抑郁症分数。将一百四十四名患者分配给活性或假刺激组。主要结果,平均视觉模拟量表降低,在每日会话期间,活性刺激组(平均值,8.0)和假组(9.2)之间的显着不同(p = 0.58)。二次结果在2组之间没有显着差异。与Sham相比,在连续每周RTMS中注册的患者在活性刺激组中取得了更多的疼痛缓解(P <0.01)。没有观察到严重的不良事件。该试验中使用的刺激条件的刺激条件的五个日常会话在整个研究人口中的短期疼痛缓解方面无效。应调查长期管理对响应者的临床使用RTMS在未来的试验中的临床应用。

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