Vagus nerve stimulation for pediatric patients with intractable epilepsy between 3 and 6 years of age: study protocol for a double-blind, randomized control trial

Recent clinical observations have reported the potential benefit of vagus nerve stimulation (VNS) as an adjunctive therapy for pediatric epilepsy. Preliminary evidence suggests that VNS treatment is effective for seizure reduction and mental development in young participants between 3 and 6 years of...

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Veröffentlicht in:Current controlled trials in cardiovascular medicine 2019-01, Vol.20 (1), p.44-44, Article 44
Hauptverfasser: Ji, Taoyun, Yang, Zhao, Liu, Qingzhu, Liao, Jianxiang, Yin, Fei, Chen, Yanhui, Zou, Liping, Li, Baomin, Gao, Yuxing, Shu, Xiaomei, Huang, Shaoping, Gao, Feng, Liang, Jianmin, Lin, Su Fang, Peng, Jing, Song, Shiwei, Wang, Jing, Che, Chao, Sun, Wenxiu, Tian, Maoqiang, Yang, Lin, Hua, Yi, Hao, Yunpeng, Cai, Lixin, Li, Luming, Jiang, Yuwu
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Sprache:eng
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Zusammenfassung:Recent clinical observations have reported the potential benefit of vagus nerve stimulation (VNS) as an adjunctive therapy for pediatric epilepsy. Preliminary evidence suggests that VNS treatment is effective for seizure reduction and mental development in young participants between 3 and 6 years of age who suffer from intractable epilepsy. However, robust clinical evidence for quantifying the difference of the efficacy and safety of VNS treatment in this specific patient population has yet to be reported. A two-armed, multicenter, randomized, double-blind, prospective trial will be carried out to evaluate whether VNS is beneficial and safe for pediatric epilepsy. Pediatric participants aged between 3 to 6 years old with intractable epilepsy will be recruited and randomly assigned to experimental and control groups with a 1:1 allocation using a computer-generating randomization schedule. Before enrollment, informed consent will be signed by the parents of the participants and the study researchers. Participants in the experimental group will receive electrical stimulation over 24 weeks under standard stimulation parameters. Participants in the control group will not receive any stimulation during the 12 weeks of the double-blind period. The guardians of the participants are required to keep a detailed diary to record seizure activity. Outcome assessments including seizure frequency, Gesell Mental Developmental Scale scores, use of antiepileptic drugs and dosages, and adverse events will be collected at baseline, 6, 12, 18 and/or 24 weeks after electrical stimulation is initiated. The effects of treatment will be analyzed with time and treatment group comparisons. This trial will evaluate quantitative differences in efficacy and safety with/without VNS treatment for pediatric participants aged between 3 to 6 years with intractable epilepsy and will explore whether the current age range of VNS therapy can be expanded. ClinicalTrials.gov, ID: NCT03062514 , Registered on 23 February 2017.
ISSN:1745-6215
1745-6215
DOI:10.1186/s13063-018-3087-4