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Yishenyangsui granule for degenerative cervical myelopathy: a randomized, double-blind, placebo-controlled trial with long-term follow-up

Affiliation
Wangjing Hospital ,China Academy of Chinese Medical Sciences ,Beijing ,China
Yin, He;
Affiliation
Wangjing Hospital ,China Academy of Chinese Medical Sciences ,Beijing ,China
Chen, Xin;
Affiliation
Wangjing Hospital ,China Academy of Chinese Medical Sciences ,Beijing ,China
Liu, Zhiwei;
Affiliation
Wangjing Hospital ,China Academy of Chinese Medical Sciences ,Beijing ,China
Xu, Bo;
Affiliation
Wangjing Hospital ,China Academy of Chinese Medical Sciences ,Beijing ,China
Jin, Zhefeng;
Affiliation
Key Laboratory of Chinese Internal Medicine of Ministry of Education ,Beijing University of Chinese Medicine Affiliated Dongzhimen Hospital ,Beijing ,China
Liu, Yan;
Affiliation
Wangjing Hospital ,China Academy of Chinese Medical Sciences ,Beijing ,China
Qi, Baoyu;
Affiliation
Wangjing Hospital ,China Academy of Chinese Medical Sciences ,Beijing ,China
Tang, Bin;
Affiliation
First Teaching Hospital of Tianjin University of Traditional Chinese Medicine ,Tianjin ,China
Wang, Ping;
Affiliation
Spine Department ,Beijing Hospital of Traditional Chinese Medicine ,Beijing ,China
Xu, Fanping;
Affiliation
Wangjing Hospital ,China Academy of Chinese Medical Sciences ,Beijing ,China
Wei, Xu;
Affiliation
Wangjing Hospital ,China Academy of Chinese Medical Sciences ,Beijing ,China
Yu, Jie;
Affiliation
Wangjing Hospital ,China Academy of Chinese Medical Sciences ,Beijing ,China
Zhu, Liguo

Objective This randomized controlled trial aims to evaluate the efficacy and safety of Yishenyangsui granule for treating Degenerative Cervical Myelopathy. Materials and methods A randomized, double-blind, placebo-controlled clinical trial was conducted with 152 participants recruited from three centers and randomly assigned to receive either Yishenyangsui granule or placebo. The Japanese Orthopaedic Association (JOA) score and Neck Disability Index (NDI) score were evaluated for 32 weeks. Patient-reported outcomes including surgical treatment data, re-treatment data, and patient-reported condition were collected for long-term follow-up. This trial was approved by the ethics committee of WangJing Hospital of China Academy of Chinese Medical Sciences (WJEC-KT-2016-004-P001) and was registered at the Chinese Clinical Trials Registry (ChiCTR-INR-16009723) on 03 November 2016 (Check out at https://www.chictr.org.cn/indexEN.html for a more comprehensive overview). Results The results showed that the improvement in JOA score at week 8 was significantly better in the Yishenyangsui granule group than in the placebo group (1.47 vs. 0.43; P < 0.001). Furthermore, improvements in motor function of upper/lower extremities, sensory function of upper extremities, reading ability, and recreation domain scores were also significantly superior in the Yishenyangsui granule group compared to the placebo group (P < 0.05). Long-term follow-up outcomes revealed no statistical differences between groups regarding surgical treatment data or patient-reported condition (P > 0.05). However, there was a significant difference detected in re-treatment data between groups with a lower rate observed among those receiving Yishenyangsui granule compared to those receiving placebo [25 (43.10%) vs. 40 (68.97%); P = 0.033], indicating its effectiveness for treating mild-to-moderate Degenerative Cervical Myelopathy. Conclusion Yishenyangsui granule was effective in treating mild to moderate Degenerative Cervical Myelopathy. The participants have improved long-term outcomes. Clinical Trials Registration https://www.chictr.org.cn/indexEN.html , identifier ChiCTR-INR-16009723.

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License Holder: Copyright © 2025 Yin, Chen, Liu, Xu, Jin, Liu, Qi, Tang, Wang, Xu, Wei, Yu and Zhu.

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