Clinical study of a micro-implantable pulse generator for the treatment of peripheral neuropathic pain: 12-month results from the COMFORT-randomized controlled trial

医学 随机对照试验 经皮神经电刺激 不利影响 神经病理性疼痛 外围设备 慢性疼痛 随机化 临床试验 麻醉 物理疗法 外科 内科学 替代医学 病理
作者
John Hatheway,Alexander Hersel,Mitchell P. Engle,Genaro Gutierrez,Vishal Khemlani,Leonardo Kapural,Gregory A. Moore,Reginald Ajakwe,Drew Trainor,Jennifer M. Hah,Peter S. Staats,James Makous,Gary Heit,Shilpa Kottalgi,Mehul J. Desai
出处
期刊:Regional Anesthesia and Pain Medicine [BMJ]
卷期号:: rapm-106099 被引量:1
标识
DOI:10.1136/rapm-2024-106099
摘要

Background There is paucity of data from randomized controlled trials supporting the use of peripheral nerve stimulation, a well-established therapy for the treatment of chronic pain. This study was undertaken, in part, to provide randomized controlled trial data in support of patient access to appropriate peripheral nerve stimulation therapy. The COMFORT study is the first large, postmarket, multicenter randomized controlled trials investigating the use of a Food and Drug Administration-cleared micro-implantable pulse generator (IPG) for treating chronic pain via peripheral nerve stimulation therapy. Methods Consented, eligible subjects were randomized to either the active arm, which received peripheral nerve stimulation and conventional medical management, or the control arm, which received conventional medical management alone and were allowed to cross over to the active arm, after 3 months. Pain and patient-reported outcomes were captured. Therapy responders were subjects who achieved at least a 50% reduction in pain scores compared with baseline. We are reporting the 12-month results of this 36-month study. Results At 12 months, the responder rate was 87% with a 69% average reduction in pain compared with baseline (7.5±1.2 to 2.3±1.7; p<0.001). Statistical significance was achieved for all patient-reported outcomes. There was an excellent safety profile with no serious adverse device effects or reports of pocket pain. A majority of subjects used unique programming options and found this device easy to use and comfortable to wear. Conclusions These 12-month results are consistent with previously reported 6-month outcomes from this study, showing durability of peripheral nerve stimulation treatment with the micro-IPG system; subjects realized sustained large reduction in pain and improvement in patient-reported outcomes following treatment with this micro-IPG system. Trial registration number NCT05287373 .

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