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Improving Stem Cell Clinical Trial Design and Conduct: Development of a Quality Assessment Tool for Stem Cell Clinical Trials

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机构: [1]Shanghai Jiao Tong Univ, Sch Med, Shanghai Tongren Hosp, Hongqiao Int Inst Med, Shanghai, Peoples R China [2]Shanghai Jiao Tong Univ, Sch Med, Fac Publ Hlth, Shanghai, Peoples R China [3]Shanghai Jiao Tong Univ, Sch Med, Clin Res Inst, Shanghai, Peoples R China [4]China Med Biotech Assoc, Beijing 100022, Peoples R China [5]Shanghai Hosp Dev Ctr, Shanghai Clin Res Promot & Dev Ctr, Shanghai 200041, Peoples R China
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Background. Clinical trials are at the cornerstone of evidence-based stem cell therapies, but the quality assessment for designing and conduct these sometimes-complex studies are scarce of evidence. This study is aimed at developing a handy quality assessment tool for stem cell clinical trials, enhancing capacity of the self-regulate overall quality, and participating protection. Methods. The framework of quality assessment tool was based on the PQRS (progress-quality-regulation-scientific) quality assessment tool, and detailed quality indicators were developed by leader group discussion, expert consulting, and literature review. Stem cell clinical trials were retrieved from the International Clinical Trials Registry Platform, and corresponding quality indicators were assessed and extracted. The validity and feasibility of conceptual quality assessment tool were further evaluated by using structural equation modeling. Results. The quality assessment tool for stem cell clinical trials contains four critical quality attributes, including participant protection, scientific value, quality control, and stem cell products, and 9 observed quality indicators. From 11 primary clinical trial registries in the International Clinical Trials Registry Platform, 9410 stem cell trial registrations were identified, and 1036 studies were eligible for publications and protocols screening. After reviewed full text, 37 studies were included in the validity and feasibility evaluation: 32 studies were completed, and 3 studies terminated early. Most of the studies (83.79%) were in the early phase, and 63.16% of the studies were investigator-initiated trial. To further tested for validity, the critical quality attributes and quality indicators (QIs) between expertise further validated by the SEM method, which showed a good fit for the model (chi-square=26.008; P=0.353; TLI=0.967; CFI=0.978; RMSEA=0.048). Compared with exploratory trials, evaluating using the quality assessment tool, confirmatory trials performed similarly in participant protection, scientific value, and quality control, but lower in stem cell products. Conclusions. The results of critical quality attributes and quality indicators between expertise and confirmatory validation analysis are basically consistent, indicating the feasibility and validity of applying this quality assessment tool for overall quality evaluation of stem cell trials.

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出版当年[2019]版:
大类 | 2 区 医学
小类 | 3 区 细胞与组织工程
最新[2025]版:
大类 | 4 区 医学
小类 | 4 区 细胞与组织工程
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出版当年[2018]版:
Q2 CELL & TISSUE ENGINEERING
最新[2023]版:
Q2 CELL & TISSUE ENGINEERING

影响因子: 最新[2023版] 最新五年平均 出版当年[2018版] 出版当年五年平均 出版前一年[2017版] 出版后一年[2019版]

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第一作者机构: [1]Shanghai Jiao Tong Univ, Sch Med, Shanghai Tongren Hosp, Hongqiao Int Inst Med, Shanghai, Peoples R China [2]Shanghai Jiao Tong Univ, Sch Med, Fac Publ Hlth, Shanghai, Peoples R China [3]Shanghai Jiao Tong Univ, Sch Med, Clin Res Inst, Shanghai, Peoples R China
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通讯机构: [1]Shanghai Jiao Tong Univ, Sch Med, Shanghai Tongren Hosp, Hongqiao Int Inst Med, Shanghai, Peoples R China [2]Shanghai Jiao Tong Univ, Sch Med, Fac Publ Hlth, Shanghai, Peoples R China [5]Shanghai Hosp Dev Ctr, Shanghai Clin Res Promot & Dev Ctr, Shanghai 200041, Peoples R China
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