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Resource use, costs, and approval times for planning and preparing a randomized clinical trial before and after the implementation of the new Swiss human research legislation

BACKGROUND: The preparation of a randomized controlled trial (RCT) requires substantial resources and the administrative processes can be burdensome. To facilitate the conduct of RCTs it is important to better understand cost drivers. In January 2014 the enactment of the new Swiss Legislation on Hum...

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Autores principales: Speich, Benjamin, Schur, Nadine, Gryaznov, Dmitry, von Niederhäusern, Belinda, Hemkens, Lars G., Schandelmaier, Stefan, Amstutz, Alain, Kasenda, Benjamin, Pauli-Magnus, Christiane, Ojeda-Ruiz, Elena, Tomonaga, Yuki, McCord, Kimberly, Nordmann, Alain, von Elm, Erik, Briel, Matthias, Schwenkglenks, Matthias
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329511/
https://www.ncbi.nlm.nih.gov/pubmed/30633776
http://dx.doi.org/10.1371/journal.pone.0210669
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author Speich, Benjamin
Schur, Nadine
Gryaznov, Dmitry
von Niederhäusern, Belinda
Hemkens, Lars G.
Schandelmaier, Stefan
Amstutz, Alain
Kasenda, Benjamin
Pauli-Magnus, Christiane
Ojeda-Ruiz, Elena
Tomonaga, Yuki
McCord, Kimberly
Nordmann, Alain
von Elm, Erik
Briel, Matthias
Schwenkglenks, Matthias
author_facet Speich, Benjamin
Schur, Nadine
Gryaznov, Dmitry
von Niederhäusern, Belinda
Hemkens, Lars G.
Schandelmaier, Stefan
Amstutz, Alain
Kasenda, Benjamin
Pauli-Magnus, Christiane
Ojeda-Ruiz, Elena
Tomonaga, Yuki
McCord, Kimberly
Nordmann, Alain
von Elm, Erik
Briel, Matthias
Schwenkglenks, Matthias
author_sort Speich, Benjamin
collection PubMed
description BACKGROUND: The preparation of a randomized controlled trial (RCT) requires substantial resources and the administrative processes can be burdensome. To facilitate the conduct of RCTs it is important to better understand cost drivers. In January 2014 the enactment of the new Swiss Legislation on Human Research (LHR) considerably changed the regulatory framework in Switzerland. We assess if the new LHR was associated with change in (i) resource use and costs to prepare an RCT, and (ii) approval times with research ethics committees (RECs) and the regulatory authority Swissmedic. METHODS: We surveyed investigators of RCTs which were approved by RECs in 2012 or in 2016 and asked for RCT preparation costs using a pre-specified item list. Additionally, we collected approval times from RECs and Swissmedic. RESULTS: The response rates of the investigator survey were 8.3% (19/228) for 2012 and 16.5% (47/285) in 2016. The median preparation cost of an RCT was USD 72,400 (interquartile range [IQR]: USD 59,500–87,700; n = 18) in 2012 and USD 72,600 (IQR: USD 42,800–169,600; n = 35) in 2016. For single centre RCTs a median REC approval time of 82 (IQR: 49–107; n = 38) days in 2012 and 92 (IQR: 65–131; n = 63) days in 2016 was observed. The median Swissmedic approval time for any clinical trial was 27 (IQR: 19–51; n = 213) days in 2012 and 49 (IQR: 36–67; n = 179) days in 2016. The total duration for achieving RCT approval from both authorities (REC and Swissmedic) in the parallel submission procedure applied in 2016 could not be assessed. CONCLUSION: Based on limited data the costs to plan and prepare RCTs in Switzerland were approximately USD 72,000 in 2012 and 2016. For effective and valid research on costs and approval times of RCTs a greater willingness to share cost information among investigators and more collaboration between stakeholders with data linkage is necessary.
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spelling pubmed-63295112019-02-01 Resource use, costs, and approval times for planning and preparing a randomized clinical trial before and after the implementation of the new Swiss human research legislation Speich, Benjamin Schur, Nadine Gryaznov, Dmitry von Niederhäusern, Belinda Hemkens, Lars G. Schandelmaier, Stefan Amstutz, Alain Kasenda, Benjamin Pauli-Magnus, Christiane Ojeda-Ruiz, Elena Tomonaga, Yuki McCord, Kimberly Nordmann, Alain von Elm, Erik Briel, Matthias Schwenkglenks, Matthias PLoS One Research Article BACKGROUND: The preparation of a randomized controlled trial (RCT) requires substantial resources and the administrative processes can be burdensome. To facilitate the conduct of RCTs it is important to better understand cost drivers. In January 2014 the enactment of the new Swiss Legislation on Human Research (LHR) considerably changed the regulatory framework in Switzerland. We assess if the new LHR was associated with change in (i) resource use and costs to prepare an RCT, and (ii) approval times with research ethics committees (RECs) and the regulatory authority Swissmedic. METHODS: We surveyed investigators of RCTs which were approved by RECs in 2012 or in 2016 and asked for RCT preparation costs using a pre-specified item list. Additionally, we collected approval times from RECs and Swissmedic. RESULTS: The response rates of the investigator survey were 8.3% (19/228) for 2012 and 16.5% (47/285) in 2016. The median preparation cost of an RCT was USD 72,400 (interquartile range [IQR]: USD 59,500–87,700; n = 18) in 2012 and USD 72,600 (IQR: USD 42,800–169,600; n = 35) in 2016. For single centre RCTs a median REC approval time of 82 (IQR: 49–107; n = 38) days in 2012 and 92 (IQR: 65–131; n = 63) days in 2016 was observed. The median Swissmedic approval time for any clinical trial was 27 (IQR: 19–51; n = 213) days in 2012 and 49 (IQR: 36–67; n = 179) days in 2016. The total duration for achieving RCT approval from both authorities (REC and Swissmedic) in the parallel submission procedure applied in 2016 could not be assessed. CONCLUSION: Based on limited data the costs to plan and prepare RCTs in Switzerland were approximately USD 72,000 in 2012 and 2016. For effective and valid research on costs and approval times of RCTs a greater willingness to share cost information among investigators and more collaboration between stakeholders with data linkage is necessary. Public Library of Science 2019-01-11 /pmc/articles/PMC6329511/ /pubmed/30633776 http://dx.doi.org/10.1371/journal.pone.0210669 Text en © 2019 Speich et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Speich, Benjamin
Schur, Nadine
Gryaznov, Dmitry
von Niederhäusern, Belinda
Hemkens, Lars G.
Schandelmaier, Stefan
Amstutz, Alain
Kasenda, Benjamin
Pauli-Magnus, Christiane
Ojeda-Ruiz, Elena
Tomonaga, Yuki
McCord, Kimberly
Nordmann, Alain
von Elm, Erik
Briel, Matthias
Schwenkglenks, Matthias
Resource use, costs, and approval times for planning and preparing a randomized clinical trial before and after the implementation of the new Swiss human research legislation
title Resource use, costs, and approval times for planning and preparing a randomized clinical trial before and after the implementation of the new Swiss human research legislation
title_full Resource use, costs, and approval times for planning and preparing a randomized clinical trial before and after the implementation of the new Swiss human research legislation
title_fullStr Resource use, costs, and approval times for planning and preparing a randomized clinical trial before and after the implementation of the new Swiss human research legislation
title_full_unstemmed Resource use, costs, and approval times for planning and preparing a randomized clinical trial before and after the implementation of the new Swiss human research legislation
title_short Resource use, costs, and approval times for planning and preparing a randomized clinical trial before and after the implementation of the new Swiss human research legislation
title_sort resource use, costs, and approval times for planning and preparing a randomized clinical trial before and after the implementation of the new swiss human research legislation
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6329511/
https://www.ncbi.nlm.nih.gov/pubmed/30633776
http://dx.doi.org/10.1371/journal.pone.0210669
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