Author: gao song; meng qun cheng; xian wen wei
Title: Advance of Novel Coronavirus Registration Clinical Trial Document date: 2020_3_20
ID: fk2wc715_40
Snippet: In addition, the study period is also "time-effective". If a clinical study is long, it may not make much sense in terms of public health emergencies to respond to the outbreak. From the statistical data, it can be seen that the time limit for completing most of the clinical studies of COVID-19 is concentrated within 4-12 months, and very few studies are completed within 1 month. The clinical research to deal with the epidemic is to race against .....
Document: In addition, the study period is also "time-effective". If a clinical study is long, it may not make much sense in terms of public health emergencies to respond to the outbreak. From the statistical data, it can be seen that the time limit for completing most of the clinical studies of COVID-19 is concentrated within 4-12 months, and very few studies are completed within 1 month. The clinical research to deal with the epidemic is to race against the virus and the epidemic. This time limit seems too long. Is it possible to conduct mid-term analysis or other adaptive, new design methods? Clinical trial statistics need to be continuously developed All rights reserved. No reuse allowed without permission.
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