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Statistical design considerations for pilot studies transitioning therapies from the bench to the bedside

Pilot studies are often used to transition therapies developed using animal models to a clinical setting. Frequently, the focus of such trials is on estimating the safety in terms of the occurrence of certain adverse events. With relatively small sample sizes, the probability of observing even relat...

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Detalles Bibliográficos
Autores principales: Carter, Rickey E, Woolson, Robert F
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC527875/
https://www.ncbi.nlm.nih.gov/pubmed/15511289
http://dx.doi.org/10.1186/1479-5876-2-37
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author Carter, Rickey E
Woolson, Robert F
author_facet Carter, Rickey E
Woolson, Robert F
author_sort Carter, Rickey E
collection PubMed
description Pilot studies are often used to transition therapies developed using animal models to a clinical setting. Frequently, the focus of such trials is on estimating the safety in terms of the occurrence of certain adverse events. With relatively small sample sizes, the probability of observing even relatively common events is low; however, inference on the true underlying event rate is still necessary even when no events of interest are observed. The exact upper limit to the event rate is derived and illustrated graphically. In addition, the simple algebraic expression for the confidence bound is seen to be useful in the context of planning studies.
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spelling pubmed-5278752004-11-14 Statistical design considerations for pilot studies transitioning therapies from the bench to the bedside Carter, Rickey E Woolson, Robert F J Transl Med Commentary Pilot studies are often used to transition therapies developed using animal models to a clinical setting. Frequently, the focus of such trials is on estimating the safety in terms of the occurrence of certain adverse events. With relatively small sample sizes, the probability of observing even relatively common events is low; however, inference on the true underlying event rate is still necessary even when no events of interest are observed. The exact upper limit to the event rate is derived and illustrated graphically. In addition, the simple algebraic expression for the confidence bound is seen to be useful in the context of planning studies. BioMed Central 2004-10-28 /pmc/articles/PMC527875/ /pubmed/15511289 http://dx.doi.org/10.1186/1479-5876-2-37 Text en Copyright © 2004 Carter and Woolson; 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 Commentary
Carter, Rickey E
Woolson, Robert F
Statistical design considerations for pilot studies transitioning therapies from the bench to the bedside
title Statistical design considerations for pilot studies transitioning therapies from the bench to the bedside
title_full Statistical design considerations for pilot studies transitioning therapies from the bench to the bedside
title_fullStr Statistical design considerations for pilot studies transitioning therapies from the bench to the bedside
title_full_unstemmed Statistical design considerations for pilot studies transitioning therapies from the bench to the bedside
title_short Statistical design considerations for pilot studies transitioning therapies from the bench to the bedside
title_sort statistical design considerations for pilot studies transitioning therapies from the bench to the bedside
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC527875/
https://www.ncbi.nlm.nih.gov/pubmed/15511289
http://dx.doi.org/10.1186/1479-5876-2-37
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