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The statistical analysis of a clinical trial when a protocol amendment changed the inclusion criteria
BACKGROUND: Sometimes, protocol amendments that change the inclusion and exclusion criteria are required in clinical trials. Then, the patient populations before and after the amendment may differ. METHODS: We propose to perform separate statistical tests for the different phases, i.e. for the patie...
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2008
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2359757/ https://www.ncbi.nlm.nih.gov/pubmed/18397525 http://dx.doi.org/10.1186/1471-2288-8-16 |
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author | Lösch, Christian Neuhäuser, Markus |
author_facet | Lösch, Christian Neuhäuser, Markus |
author_sort | Lösch, Christian |
collection | PubMed |
description | BACKGROUND: Sometimes, protocol amendments that change the inclusion and exclusion criteria are required in clinical trials. Then, the patient populations before and after the amendment may differ. METHODS: We propose to perform separate statistical tests for the different phases, i.e. for the patients recruited before and after the amendment, and to combine the tests using Fisher's combination test. After a significant combination test a multiple testing procedure can be applied to identify the phase(s) to which a proof of efficacy refers. We assume that the amendment(s) are not based on any type of unblinded data. The proposed method is investigated within a simulation study. RESULTS: The proposed combination approach is superior to the 'naïve' strategy to ignore the differences between the phases and pooling the data to perform just one statistical test. This superiority disappears when there are hardly any differences between the two phases. CONCLUSION: When one or more protocol amendments change the inclusion and exclusion criteria, one should realize that the populations may differ. In this case, separate tests for the different phases together with a combination test are a powerful method that can be applied in a variety of settings. The (first) amendment should specify the combination test to be applied in order to combine the different phases. |
format | Text |
id | pubmed-2359757 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2008 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-23597572008-05-01 The statistical analysis of a clinical trial when a protocol amendment changed the inclusion criteria Lösch, Christian Neuhäuser, Markus BMC Med Res Methodol Research Article BACKGROUND: Sometimes, protocol amendments that change the inclusion and exclusion criteria are required in clinical trials. Then, the patient populations before and after the amendment may differ. METHODS: We propose to perform separate statistical tests for the different phases, i.e. for the patients recruited before and after the amendment, and to combine the tests using Fisher's combination test. After a significant combination test a multiple testing procedure can be applied to identify the phase(s) to which a proof of efficacy refers. We assume that the amendment(s) are not based on any type of unblinded data. The proposed method is investigated within a simulation study. RESULTS: The proposed combination approach is superior to the 'naïve' strategy to ignore the differences between the phases and pooling the data to perform just one statistical test. This superiority disappears when there are hardly any differences between the two phases. CONCLUSION: When one or more protocol amendments change the inclusion and exclusion criteria, one should realize that the populations may differ. In this case, separate tests for the different phases together with a combination test are a powerful method that can be applied in a variety of settings. The (first) amendment should specify the combination test to be applied in order to combine the different phases. BioMed Central 2008-04-08 /pmc/articles/PMC2359757/ /pubmed/18397525 http://dx.doi.org/10.1186/1471-2288-8-16 Text en Copyright © 2008 Lösch and Neuhäuser; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Lösch, Christian Neuhäuser, Markus The statistical analysis of a clinical trial when a protocol amendment changed the inclusion criteria |
title | The statistical analysis of a clinical trial when a protocol amendment changed the inclusion criteria |
title_full | The statistical analysis of a clinical trial when a protocol amendment changed the inclusion criteria |
title_fullStr | The statistical analysis of a clinical trial when a protocol amendment changed the inclusion criteria |
title_full_unstemmed | The statistical analysis of a clinical trial when a protocol amendment changed the inclusion criteria |
title_short | The statistical analysis of a clinical trial when a protocol amendment changed the inclusion criteria |
title_sort | statistical analysis of a clinical trial when a protocol amendment changed the inclusion criteria |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2359757/ https://www.ncbi.nlm.nih.gov/pubmed/18397525 http://dx.doi.org/10.1186/1471-2288-8-16 |
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