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- W2347810615 abstract "Objective:To assess the feasibility of statistical methods in elimination of possible confounding factors in clinical trial settings.Methods:Several suitable statistical methods to control confounding factors,such as central effect,covariate,and so on,were exampled.Results:In general,these confounding factors were associated with the disease under study and with the exposure(of the subjects) to some agents or conditions.Comprehensive data collected by correct statistical strategies were essential to eliminate possible confounding fallaciousness.This includes not only prospectively collected data on therapy use,but also information on access,healthcare utilization and practices,and adherence.Conclusion:A more elaborate statistical analysis rendered better agreement in fully mimicking what outcomes of study drugs accomplished in a clinical trial setting." @default.
- W2347810615 created "2016-06-24" @default.
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- W2347810615 date "2005-01-01" @default.
- W2347810615 modified "2023-09-26" @default.
- W2347810615 title "Strategies to control confounding factors in clinical trials" @default.
- W2347810615 hasPublicationYear "2005" @default.
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