Stimdia Medical, Inc, 1355 Mendota Heights Road, Suite 300, Mendota Heights, MN, 55120, USA.
NAMSA, 6750 Wales Rd, Northwood, OH, 43619, USA.
Trials. 2024 Aug 2;25(1):519. doi: 10.1186/s13063-024-08355-8.
In the United States in 2017, there were an estimated 903,745 hospitalizations involving mechanical ventilation (MV). Complications from ventilation can result in longer hospital stays, increased risk of disability, and increased healthcare costs. It has been hypothesized that electrically pacing the diaphragm by phrenic nerve stimulation during mechanical ventilation may minimize or reverse diaphragm dysfunction, resulting in faster weaning.
The ReInvigorate Trial is a prospective, multicenter, randomized, controlled clinical trial evaluating the safety and efficacy of Stimdia's pdSTIM System for facilitating weaning from MV. The pdSTIM system employs percutaneously placed multipolar electrodes to stimulate the cervical phrenic nerves and activate contraction of the diaphragm bilaterally. Patients who were on mechanical ventilation for at least 96 h and who failed at least one weaning attempt were considered for enrollment in the study. The primary efficacy endpoint was the time to successful liberation from mechanical ventilation (treatment vs. control). Secondary endpoints will include the rapid shallow breathing index and other physiological and system characteristics. Safety will be summarized for both primary and additional analyses. All endpoints will be evaluated at 30 days or at the time of removal of mechanical ventilation, whichever is first.
This pivotal study is being conducted under an investigational device exception with the U.S. Food and Drug Administration. The technology being studied could provide a first-of-kind therapy for difficult-to-wean patients on mechanical ventilation in an intensive care unit setting.
Clinicaltrials.gov, NCT05998018 , registered August 2023.
2017 年在美国,估计有 903745 例涉及机械通气(MV)的住院治疗。通气并发症可导致住院时间延长、残疾风险增加和医疗保健费用增加。人们假设,在机械通气期间通过膈神经刺激对膈进行电起搏可以最小化或逆转膈功能障碍,从而更快地脱机。
ReInvigorate 试验是一项前瞻性、多中心、随机、对照临床试验,评估了 Stimdia 的 pdSTIM 系统促进 MV 脱机的安全性和有效性。pdSTIM 系统采用经皮放置的多极电极刺激颈膈神经,双侧激活膈的收缩。至少接受 96 小时机械通气且至少一次脱机尝试失败的患者被考虑入组该研究。主要疗效终点是成功从机械通气中解脱的时间(治疗组与对照组)。次要终点将包括快速浅呼吸指数和其他生理和系统特征。安全性将在主要和其他分析中进行总结。所有终点都将在 30 天或机械通气去除时进行评估,以先到者为准。
这项关键研究是在美国食品和药物管理局的调查设备例外情况下进行的。正在研究的技术可以为 ICU 环境中难以脱机的机械通气患者提供一种首创的治疗方法。
Clinicaltrials.gov,NCT05998018,于 2023 年 8 月注册。