Missing data in clinical trials can result in biased treatment effect estimates and tests if the analysis includes only the observed data. Two simple methods of compensating for this potential bias in trials with a binary endpoint were suggested by Wittes et al. (Statist. Med. 8 (1989) 415-425). We study the statistical properties of these procedures and show that they are robust against certain model departures. (C) 2001 Elsevier Science B.V. All rights reserved.
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Imperial Coll London, Imperial Clin Trials Unit, Stadium House,68 Wood Lane, London W12 7RH, EnglandImperial Coll London, Imperial Clin Trials Unit, Stadium House,68 Wood Lane, London W12 7RH, England
Cro, Suzie
Morris, Tim P.
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UCL, MRC Clin Trials Unit UCL, London, England
LSHTM, Med Stat Dept, London, EnglandImperial Coll London, Imperial Clin Trials Unit, Stadium House,68 Wood Lane, London W12 7RH, England
Morris, Tim P.
Kenward, Michael G.
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机构:Imperial Coll London, Imperial Clin Trials Unit, Stadium House,68 Wood Lane, London W12 7RH, England
Kenward, Michael G.
Carpenter, James R.
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UCL, MRC Clin Trials Unit UCL, London, England
LSHTM, Med Stat Dept, London, EnglandImperial Coll London, Imperial Clin Trials Unit, Stadium House,68 Wood Lane, London W12 7RH, England
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Merck Res Labs, Late Dev Clin Biostat, 351 N Sumneytown Pike,UG1CD 44, N Wales, PA 19454 USAMerck Res Labs, Late Dev Clin Biostat, 351 N Sumneytown Pike,UG1CD 44, N Wales, PA 19454 USA
Liu, G. Frank
Pang, Lei
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Merck Res Labs, Late Dev Clin Biostat, 351 N Sumneytown Pike,UG1CD 44, N Wales, PA 19454 USAMerck Res Labs, Late Dev Clin Biostat, 351 N Sumneytown Pike,UG1CD 44, N Wales, PA 19454 USA