An overview of practical approaches for handling missing data in clinical trials

CM DeSouza, ATR Legedza… - Journal of …, 2009 - Taylor & Francis
For a variety of reasons including poorly designed case report forms (CRFs), incomplete or
invalid CRF data entries, and premature treatment or study discontinuations, missing data is …
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An Overview of Practical Approaches for Handling Missing Data in Clinical Trials

C DeSouza, A Legedza… - Journal of …, 2009 - ingentaconnect.com
For a variety of reasons including poorly designed case report forms (CRFs), incomplete or
invalid CRF data entries, and premature treatment or study discontinuations, missing data is …

[引用][C] An Overview of Practical Approaches for Handling Missing Data in Clinical Trials

CM DeSouza, ATR Legedza, AJ Sankoh - Journal of Biopharmaceutical …, 2009 - cir.nii.ac.jp
An Overview of Practical Approaches for Handling Missing Data in Clinical Trials | CiNii
Research CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索フォームへ移動 …

An overview of practical approaches for handling missing data in clinical trials

CM DeSouza, ATR Legedza… - Journal of …, 2009 - pubmed.ncbi.nlm.nih.gov
For a variety of reasons including poorly designed case report forms (CRFs), incomplete or
invalid CRF data entries, and premature treatment or study discontinuations, missing data is …

An overview of practical approaches for handling missing data in clinical trials.

CM DeSouza, AT Legedza… - Journal of …, 2009 - europepmc.org
For a variety of reasons including poorly designed case report forms (CRFs), incomplete or
invalid CRF data entries, and premature treatment or study discontinuations, missing data is …