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Sensitivity analyses using multiple imputation (MI) provide a flexible approach to assess the impact of missing data on clinical trial results. An approach that imputes missing data in the test drug group using a model built from the control group has gained attention in recent research. This control-based imputation (CBI) approach typically provides a conservative point estimate for treatment difference. However, the combined variance using Rubin's rule may over-estimate the variability. In this article, we investigate the statistical properties for some specific CBI methods, and show the relationship between CBI and delta-adjustment tipping point analysis. This relationship helps us to understand and interpret the results from CBI using MI with Rubin's rule. In addition, we propose a new sensitivity measure for assessing the robustness of the result obtained under a missing at random (MAR) assumption. Results from simulation studies and applications to longitudinal clinical trial datasets are presented as illustration.
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Liu et al. (2016) studied this question.
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