椎间盘再生临床试验为何难以完成?从发表情况和资金来源看问题

IF 3.4 3区 医学 Q1 ORTHOPEDICS JOR Spine Pub Date : 2024-05-24 DOI:10.1002/jsp2.1329
Luca Ambrosio, Giorgia Petrucci, Fabrizio Russo, Claudia Cicione, Rocco Papalia, Gianluca Vadalà, Vincenzo Denaro
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引用次数: 0

摘要

背景 慢性椎间盘源性腰背痛(LBP)给全球带来了沉重负担,但直接针对潜在退行性病变过程的有效治疗干预措施却仍未见踪影。椎间盘内注射细胞疗法在临床前研究中取得了可喜的成果,因此越来越多的临床研究开始关注这种疗法。然而,大多数临床试验都未能发表,仅有的几份报告也只显示出轻微的改善。本研究的目的是分析在 ClinicalTrials.go 上注册的研究椎间盘突出症细胞疗法的前瞻性临床试验,重点是找出阻碍研究完成的关键因素,包括试验设计和资金来源。 方法 在ClinicalTrials.gov上对研究椎间盘退变引起的慢性枸杞痛的细胞疗法的前瞻性临床试验进行了系统检索。提取的数据包括研究设计、招募、实验治疗方式、调查结果、当前状态、完成日期、发表状态和资金来源。费雪精确检验评估了分类变量之间的关联,而多元逻辑回归模型则旨在确定与研究发表状态相关的潜在因素。 结果 我们的搜索发现了 26 项临床试验。其中只有 7 项(26.9%)已发表,其他标注为已完成的研究均未在 ClinicalTrials.gov 上报告任何结果。50%的纳入试验由大学资助,其余试验则由企业(38.5%)或私人机构(11.5%)赞助。实验治疗主要涉及不同来源和浓度的细胞或细胞衍生产品。含有载体(如透明质酸或纤维蛋白)的产品更多地由工业界和私人机构资助(p = 0.0112)。比较已发表和未发表研究的资金情况,以及发表情况和其他变量之间的差异并不明显。 结论 大多数探索基于细胞的椎间盘再生疗法治疗慢性腰椎间盘突出症的临床试验从未完成,只有一小部分在出版物中报告了初步数据。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Why clinical trials in disc regeneration strive to achieve completion: Insights from publication status and funding sources

Background

Chronic discogenic low back pain (LBP) poses a significant global burden, yet effective therapeutic interventions directly targeting the underlying degenerative process remain elusive. After demonstrating promising results in preclinical studies, intradiscal injection of cell-based treatments has been increasingly investigated in the clinical setting. However, most clinical trials failed to reach publication, with the few available reports showing only minor improvements. The aim of this study was to analyze the prospective clinical trials registered on ClinicalTrials.gov investigating cell therapies for LBP, with a specific emphasis on identifying critical obstacles hindering study completion, including trial design and funding sources.

Methods

A systematic search of prospective clinical trials investigating cell-based treatments for chronic LBP due to intervertebral disc degeneration was performed on ClinicalTrials.gov. Extracted data encompassed study design, recruitment, experimental treatment modalities, investigated outcomes, current status, completion date, publication status, and funding sources. Fisher's exact test assessed associations between categorical variables, while a multiple logistic regression model aimed to identify factors potentially linked to the publication status of the studies.

Results

Our search identified 26 clinical trials. Among these, only 7 (26.9%) were published, and none of the other studies marked as completed reported any results on ClinicalTrials.gov. Fifty percent of included trials were funded by universities, whereas the rest was sponsored by industry (38.5%) or private institutions (11.5%). Experimental treatments primarily involved cell-based or cell-derived products of varying sources and concentrations. Products containing carriers, such as hyaluronic acid or fibrin, were more frequently funded by industry and private organizations (p = 0.0112). No significant differences emerged when comparing published and nonpublished studies based on funding, as well as between publication status and other variables.

Conclusion

Most clinical trials exploring cell-based disc regenerative therapies for chronic LBP have never reached completion, with only a small fraction reporting preliminary data in publications.

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来源期刊
JOR Spine
JOR Spine ORTHOPEDICS-
CiteScore
6.40
自引率
18.90%
发文量
42
审稿时长
10 weeks
期刊最新文献
Is There a Positive or Negative Correlation Between Cervical Vertebral Bone Quality and Intervertebral Disc Degeneration by Pfirrmann Grading. Contemporary clinical perspectives on chronic low back pain: The biology, mechanics, etc. underpinning clinical and radiological evaluation. Assessment of Vertebral Bone Marrow Perfusion, Fat/Water Content, and Trabecular Bone Changes Using Multimodal MRI and Micro-CT in a Rat Model of Chronic Kidney Disease. Low-Frequency Cyclic Stretch Upregulates the Expression of Nuclear Factor Erythroid 2-Related Factor 2 in Human Nucleus Pulposus Cells to Inhibit the Resistin-Induced Interleukin-20 Expression. Intervertebral Disc Degeneration Mediates the Causal Effect of Genetically Predicted Diffuse Idiopathic Skeletal Hyperostosis on Spinal Stenosis: Evidence From a Mendelian Randomization Study.
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