Doi Ryoichiro, Miyazaki Takuro, Tsuchiya Tomoshi, Matsumoto Keitaro, Tomoshige Koichi, Machino Ryusuke, Mizoguchi Satoshi, Matsumoto Takamune, Yamaguchi Keita, Takatsuna Hiroshi, Shiosakai Kazuhito, Nagayasu Takeshi
Department of Surgical Oncology, Nagasaki University Graduate School of Biomedical Sciences, Nagasaki, Japan.
Oncology Medical Science Department, Daiichi Sankyo Co., Ltd., Tokyo, Japan.
J Thorac Dis. 2021 Oct;13(10):6062-6070. doi: 10.21037/jtd-21-741.
Intercostal nerve damage due to thoracotomy or thoracoscopic manipulation is a major contributor to chronic postsurgical pain after pulmonary resection. Chronic postsurgical pain may last for months or years and can negatively impair physical functioning and daily activities. Global consensus on severe postoperative pain management is lacking, and chronic pain incidence after thoracic surgery remains high. Many patients report neuropathic pain, which can be difficult to treat with currently available therapies. The efficacy and safety of mirogabalin have been demonstrated for other types of neuropathic pain; thus, this study was planned to investigate the efficacy and safety of mirogabalin to treat neuropathic pain after thoracic surgery.
In this multicenter, randomized, open-label, parallel-group, interventional study, patients who are diagnosed with neuropathic pain following removal of a chest drain after lung resection will receive conventional therapy (non-steroidal anti-inflammatory drugs and/or acetaminophen) with or without the addition of a clinical dose of mirogabalin for 8 weeks. For patient stratification, a visual analog scale pain intensity score at baseline of <60 ≥60 mm will be used. Treatment efficacy and safety with and without the addition of mirogabalin will be assessed using a questionnaire evaluating postoperative changes in pain severity and activity. The primary study endpoint is the change in pain intensity from baseline to Week 8, measured by the visual analog scale. Additionally, the presence of chronic pain at 12 weeks after enrollment in each treatment group will be recorded.
This protocol has been reviewed and approved by the Clinical Research Review Board of Nagasaki University. Study data will be published in the Japan Registry of Clinical Trials database and peer-reviewed journals. Mirogabalin is already approved for the treatment of other types of neuropathic pain. It is anticipated that this study will provide data to elucidate the impact of mirogabalin treatment, in combination with conventional therapy, to benefit patients with neuropathic pain following thoracic surgery.
Japan Registry of Clinical Trials Identifier: jRCTs071200053.
开胸手术或胸腔镜操作导致的肋间神经损伤是肺切除术后慢性术后疼痛的主要原因。慢性术后疼痛可能持续数月或数年,会对身体功能和日常活动产生负面影响。目前缺乏关于严重术后疼痛管理的全球共识,胸外科手术后慢性疼痛的发生率仍然很高。许多患者报告有神经性疼痛,而目前可用的治疗方法可能难以治疗。米罗加巴林对其他类型的神经性疼痛的疗效和安全性已得到证实;因此,本研究旨在调查米罗加巴林治疗胸外科手术后神经性疼痛的疗效和安全性。
在这项多中心、随机、开放标签、平行组干预性研究中,肺切除术后拔除胸腔引流管后被诊断为神经性疼痛的患者将接受常规治疗(非甾体抗炎药和/或对乙酰氨基酚),加或不加临床剂量的米罗加巴林,为期8周。为了进行患者分层,将使用基线时视觉模拟量表疼痛强度评分<60或≥60mm。将使用一份评估术后疼痛严重程度和活动变化的问卷来评估加用和未加用米罗加巴林时的治疗效果和安全性。主要研究终点是通过视觉模拟量表测量的从基线到第8周疼痛强度的变化。此外,将记录每个治疗组入组后12周时慢性疼痛的存在情况。
本方案已由长崎大学临床研究审查委员会审查并批准。研究数据将发表在日本临床试验注册数据库和同行评审期刊上。米罗加巴林已被批准用于治疗其他类型的神经性疼痛。预计本研究将提供数据,以阐明米罗加巴林联合常规治疗对胸外科手术后神经性疼痛患者的益处。
日本临床试验注册标识符:jRCTs071200053。