Hu Hui-Min, Liu Wen-Hui, Li Chen, Shi Qing, Liu Chun-Hua, Liu An-Xiang, Li Yi-Fan, Zhang Yi, Mao Peng, Fan Bi-Fa
Graduate School, Beijing University of Chinese Medicine, Beijing, China.
Department of Pain Medicine, China-Japan Friendship Hospital, Beijing, China.
Front Neurol. 2025 Jan 6;15:1516262. doi: 10.3389/fneur.2024.1516262. eCollection 2024.
Postherpetic neuralgia (PHN) is a type of refractory neuropathic pain that causes significant suffering, disability, economic loss, and medical burden. In this study, we aim to evaluate the efficacy and safety of interferon (IFN)-α1b injection into the intervertebral foramen of patients with PHN.
This is a study protocol for a randomized, double-blind placebo-controlled multicenter clinical trial. A total of 200 participants with PHN from 11 hospitals will be recruited and randomly assigned to the treatment group administered with IFN-α1b and control group treated with placebo in a 1:1 ratio. Both groups will also receive oral pregabalin 150 mg twice daily and lidocaine injection into the intervertebral foramen as conventional therapy. This trial will involve a screening period, a 2-week intervention, and a 3-month follow-up. The primary outcomes will include the visual analog scale score and duration of pain relief. The secondary outcomes will include the 36-item short-form, dosage and duration of painkillers taken, viral load of varicella-zoster virus DNA, humoral cytokine level, and dosage and frequency of rescue medication. All adverse events and severe adverse events will be assessed during the study.
This study is expected to provide evidence for the efficacy and safety of IFN-α1b injection into the intervertebral foramen in patients with PHN.
https://www.chictr.org.cn/indexEN.html, identifier ChiCTR240008996.
带状疱疹后神经痛(PHN)是一种难治性神经性疼痛,会导致严重的痛苦、残疾、经济损失和医疗负担。在本研究中,我们旨在评估向PHN患者椎间孔注射干扰素(IFN)-α1b的疗效和安全性。
这是一项随机、双盲、安慰剂对照的多中心临床试验研究方案。将从11家医院招募总共200名PHN患者,并按1:1的比例随机分配到接受IFN-α1b治疗的治疗组和接受安慰剂治疗的对照组。两组还将接受口服普瑞巴林150毫克,每日两次,以及作为常规治疗的椎间孔利多卡因注射。该试验将包括一个筛查期、为期2周的干预期和3个月的随访期。主要结局将包括视觉模拟量表评分和疼痛缓解持续时间。次要结局将包括36项简短问卷、服用止痛药的剂量和持续时间、水痘-带状疱疹病毒DNA的病毒载量、体液细胞因子水平以及抢救药物的剂量和频率。在研究期间将评估所有不良事件和严重不良事件。
本研究有望为向PHN患者椎间孔注射IFN-α1b的疗效和安全性提供证据。