Sample size estimation with missing values on clinical trials

Missing data is a common problem that with extremely damaging inferences from clinical trials. This unavoidable defect is mainly due to human factors, the patient being unable to follow up and some types of observations going missing (Piantadosi, 2005). An example would be the patient refuses to und...

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Main Author: Zhang, Mengyang
Other Authors: -
Format: Final Year Project (FYP)
Language:English
Published: Nanyang Technological University 2019
Subjects:
Online Access:https://hdl.handle.net/10356/136483
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author Zhang, Mengyang
author2 -
author_facet -
Zhang, Mengyang
author_sort Zhang, Mengyang
collection NTU
description Missing data is a common problem that with extremely damaging inferences from clinical trials. This unavoidable defect is mainly due to human factors, the patient being unable to follow up and some types of observations going missing (Piantadosi, 2005). An example would be the patient refuses to undergo an examination. In this work, we compare the power of the full datasets with the power of the datasets having missing values under the 2 × 2 and 2 × 4 crossover design. In this way, we find the average percentage of the sample size that should be increased to offset the decreasing in power (original is around 80%), which is caused by 20% and 30% missing data in the tests for treatment difference and bio-equivalence. Also comparing the number of subjects (full data) which can reach 80% power through formulas and simulations. The aim of this comparison is to distinguish whether the general practices would have an overestimate or underestimate for the chosen mixed model in the analysis.
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spelling ntu-10356/1364832023-02-28T23:18:14Z Sample size estimation with missing values on clinical trials Zhang, Mengyang - School of Physical and Mathematical Sciences Yeo Kwee Poo kweepoo@ntu.edu.sg Science::Mathematics::Statistics Missing data is a common problem that with extremely damaging inferences from clinical trials. This unavoidable defect is mainly due to human factors, the patient being unable to follow up and some types of observations going missing (Piantadosi, 2005). An example would be the patient refuses to undergo an examination. In this work, we compare the power of the full datasets with the power of the datasets having missing values under the 2 × 2 and 2 × 4 crossover design. In this way, we find the average percentage of the sample size that should be increased to offset the decreasing in power (original is around 80%), which is caused by 20% and 30% missing data in the tests for treatment difference and bio-equivalence. Also comparing the number of subjects (full data) which can reach 80% power through formulas and simulations. The aim of this comparison is to distinguish whether the general practices would have an overestimate or underestimate for the chosen mixed model in the analysis. Bachelor of Science in Mathematical Sciences 2019-12-19T06:00:00Z 2019-12-19T06:00:00Z 2019 Final Year Project (FYP) https://hdl.handle.net/10356/136483 en application/pdf Nanyang Technological University
spellingShingle Science::Mathematics::Statistics
Zhang, Mengyang
Sample size estimation with missing values on clinical trials
title Sample size estimation with missing values on clinical trials
title_full Sample size estimation with missing values on clinical trials
title_fullStr Sample size estimation with missing values on clinical trials
title_full_unstemmed Sample size estimation with missing values on clinical trials
title_short Sample size estimation with missing values on clinical trials
title_sort sample size estimation with missing values on clinical trials
topic Science::Mathematics::Statistics
url https://hdl.handle.net/10356/136483
work_keys_str_mv AT zhangmengyang samplesizeestimationwithmissingvaluesonclinicaltrials