Multicenter, Double-Blinded, Randomized, Active-Sham Controlled Clinical Study Design to Assess the Safety and Effectiveness of a Novel High Frequency Electric Nerve Block System in the Treatment of Post-Amputation Pain QUEST

被引:4
|
作者
Kapural, Leonardo [1 ]
Shah, Nemath Syed [2 ]
Fang, Zi-Ping [2 ]
Mekhail, Nagy [3 ]
机构
[1] Carolinas Pain Inst, 145 Kimel Pk Dr, Winston Salem, NC 27023 USA
[2] Neuros Med Inc, Willoughby Hills, OH USA
[3] Cleveland Clin, Evidence Based Pain Management Res, Dept Pain Management, Cleveland, OH 44106 USA
来源
JOURNAL OF PAIN RESEARCH | 2022年 / 15卷
关键词
post-amputation pain; phantom pain; chronic pain; high frequency nerve block; double-blind method; randomized controlled trial; repeated measures; PHANTOM-LIMB PAIN; POSTAMPUTATION PAIN; VALIDITY; NEUROMA; TRIALS;
D O I
10.2147/JPR.S353674
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Chronic pain that follows amputation of a limb is reported as "one of the most severe pains in the human experience," due to the magnitude of tissue injury and the multiple potential of pain generators at the local peripheral, spinal, and cortical levels. The Altius (R) System was developed to deliver high-frequency nerve block (HFNB) therapy via a cuff electrode applied to the peripheral nerve(s) and an implantable pulse generator. We report a novel clinical trial design for the first study of an activeimplantable medical device in subjects with lower-limb post-amputation pain utilizing a multicenter, double-blinded, randomized, active-sham controlled clinical study protocol called QUEST, which is an ongoing investigational device exemption study to support United States Food and Drug Administration approval. Methods: The study enrollment of 180 subjects was completed in September 2021. Subjects were randomized 1:1 to the treatment group or the active-sham control group for the 3-month primary effectiveness and safety endpoints. After month 3, the active-sham control program group crossed over to the treatment program group and all subjects continued to the 12-month study endpoint. Study effectiveness success is determined by a superiority test between responder rates in the treatment and control groups at 3 months. A responder is defined as someone who experiences a 50% or greater reduction in pain scores - after a 30-minute treatment session - for more than 50% of all pain episodes in which the treatment was used. Discussion: The QUEST study design employs an active-sham control group to objectively assess the effectiveness of HFNB therapy. Additionally, the electronic diary repeated measures data collection in QUEST is expected to reduce the intra-subject variation typically observed in pain treatment studies. Finally, the longitudinal measurement of health-related quality of life and use of pain medication may, for example, show effectiveness in reducing opioid use over time.
引用
收藏
页码:1623 / 1631
页数:9
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