2024-03-29T14:18:03Zhttp://repisalud.isciii.es/oai/requestoai:repisalud.isciii.es:20.500.12105/74452023-09-28T07:26:51Zcom_20.500.12105_2053com_20.500.12105_2052com_20.500.12105_2051col_20.500.12105_2054
Repisalud
author
Speich, Benjamin
author
Schur, Nadine
author
Gryaznov, Dmitry
author
von Niederhäusern, Belinda
author
Hemkens, Lars G
author
Schandelmaier, Stefan
author
Amstutz, Alain
author
Kasenda, Benjamin
author
Pauli-Magnus, Christiane
author
Ojeda-Ruiz, Elena
author
Tomonaga, Yuki
author
McCord, Kimberly
author
Nordmann, Alain
author
von Elm, Erik
author
Briel, Matthias
author
Schwenkglenks, Matthias
funder
Federal Office of Public Health
2019-04-10T11:46:09Z
2019-04-10T11:46:09Z
2019-01-11
PLoS One. 2019 Jan 11;14(1):e0210669.
1932-6203
http://hdl.handle.net/20.500.12105/7445
30633776
10.1371/journal.pone.0210669
PloS one
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.
eng
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
journal article
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URL
https://repisalud.isciii.es/bitstream/20.500.12105/7445/1/ResourceUseCostsAnd_2019.pdf
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https://repisalud.isciii.es/bitstream/20.500.12105/7445/5/ResourceUseCostsAnd_2019.pdf.txt
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