• 1. Evidence-Based Medicine Research Centre, Jiangxi University of Chinese Medicine, Nanchang 330004, P.R.China;
  • 2. Tianjin CLINDA Medical Technology Co. Ltd., Tianjin 300457, P.R.China;
  • 3. JuFeng (TIANJIN) Medical Technology Co. Ltd., Tianjin 301700, P.R.China;
CHEN Xiaofan, Email: xiaofanci122306@163.com
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In order to promote the openness, transparency and standardization of clinical trials, improve the scientific and reliability of results, and reserve the manpower, material, and financial resources in the process of clinical trials, this study constructed an integrated intelligent management platform for clinical trials, which could carry out various types of clinical trials such as randomized controlled trials, non-randomized controlled trials, cohort studies, case-control studies, and cross-sectional studies simultaneously. The platform covers the whole process of scheme design, recruitment, follow-up, data analysis, and quality control. This paper mainly introduced the practical needs, design concept, basic framework and technical highlights to provide auxiliary tools for promoting the standardization and intelligence of clinical trials with energy saving and optimal efficiency.

Citation: CHEN Shuxian, HE Qingying, GAN Yufeng, DONG Jiawei, ZENG Zhan, ZHOU Qi, CHEN Xiaofan. Construction of an intelligent data integration platform for clinical trials based on information interaction. Chinese Journal of Evidence-Based Medicine, 2021, 21(12): 1468-1473. doi: 10.7507/1672-2531.202108044 Copy

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