A snapshot of the ongoing clinical research on COVID-19.
Identifieur interne : 001801 ( Main/Exploration ); précédent : 001800; suivant : 001802A snapshot of the ongoing clinical research on COVID-19.
Auteurs : Daniele Piovani [Italie] ; Claudia Pansieri [Italie] ; Laurent Peyrin-Biroulet [France] ; Silvio Danese [Italie] ; Stefanos Bonovas [Italie]Source :
- F1000Research [ 2046-1402 ] ; 2020.
Descripteurs français
- KwdFr :
- MESH :
- tendances : Recherche biomédicale.
- traitement médicamenteux : Infections à coronavirus, Pneumopathie virale.
- Betacoronavirus, Essais cliniques comme sujet, Humains, Pandémies.
English descriptors
- KwdEn :
- MESH :
- drug therapy : Coronavirus Infections, Pneumonia, Viral.
- trends : Biomedical Research.
- Betacoronavirus, Clinical Trials as Topic, Humans, Pandemics.
Abstract
The pandemic of coronavirus disease 2019 (COVID-19) presents an unprecedented challenge to rapidly develop new diagnostic, preventive and therapeutic strategies. Currently, thousands of new COVID-19 patients are quickly enrolled in clinical studies. We aimed to investigate the characteristics of the COVID-19 studies registered in ClinicalTrials.gov and report the extent to which they have incorporated features that are desirable for generating high-quality evidence. On April 28, 2020, a total of 945 studies on COVID-19 have been registered in ClinicalTrials.gov; 586 studies are interventional (62.0%), the most frequent allocation scheme is the parallel group assignment (437; 74.6%), they are open-label and the most common primary purpose is the research on treatment. Too many of the ongoing interventional studies have a small expected sample size and may not generate credible evidence at completion. This might lead to a delayed recognition of effective therapies that are urgently needed, and a waste of time and resources. In the COVID-19 pandemic era, it is crucial that the adoption of new diagnostic, preventive and therapeutic strategies is based upon evidence coming from well-designed, adequately powered and carefully conducted clinical trials.
DOI: 10.12688/f1000research.23843.1
PubMed: 32518636
PubMed Central: PMC7256468
Affiliations:
- France, Italie
- Grand Est, Lorraine (région)
- Nancy, Vandœuvre-lès-Nancy
- Centre hospitalier régional et universitaire de Nancy, Université de Lorraine
Links toward previous steps (curation, corpus...)
Le document en format XML
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<front><div type="abstract" xml:lang="en">The pandemic of coronavirus disease 2019 (COVID-19) presents an unprecedented challenge to rapidly develop new diagnostic, preventive and therapeutic strategies. Currently, thousands of new COVID-19 patients are quickly enrolled in clinical studies. We aimed to investigate the characteristics of the COVID-19 studies registered in ClinicalTrials.gov and report the extent to which they have incorporated features that are desirable for generating high-quality evidence. On April 28, 2020, a total of 945 studies on COVID-19 have been registered in ClinicalTrials.gov; 586 studies are interventional (62.0%), the most frequent allocation scheme is the parallel group assignment (437; 74.6%), they are open-label and the most common primary purpose is the research on treatment. Too many of the ongoing interventional studies have a small expected sample size and may not generate credible evidence at completion. This might lead to a delayed recognition of effective therapies that are urgently needed, and a waste of time and resources. In the COVID-19 pandemic era, it is crucial that the adoption of new diagnostic, preventive and therapeutic strategies is based upon evidence coming from well-designed, adequately powered and carefully conducted clinical trials.</div>
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<Abstract><AbstractText>The pandemic of coronavirus disease 2019 (COVID-19) presents an unprecedented challenge to rapidly develop new diagnostic, preventive and therapeutic strategies. Currently, thousands of new COVID-19 patients are quickly enrolled in clinical studies. We aimed to investigate the characteristics of the COVID-19 studies registered in ClinicalTrials.gov and report the extent to which they have incorporated features that are desirable for generating high-quality evidence. On April 28, 2020, a total of 945 studies on COVID-19 have been registered in ClinicalTrials.gov; 586 studies are interventional (62.0%), the most frequent allocation scheme is the parallel group assignment (437; 74.6%), they are open-label and the most common primary purpose is the research on treatment. Too many of the ongoing interventional studies have a small expected sample size and may not generate credible evidence at completion. This might lead to a delayed recognition of effective therapies that are urgently needed, and a waste of time and resources. In the COVID-19 pandemic era, it is crucial that the adoption of new diagnostic, preventive and therapeutic strategies is based upon evidence coming from well-designed, adequately powered and carefully conducted clinical trials.</AbstractText>
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<name sortKey="Danese, Silvio" sort="Danese, Silvio" uniqKey="Danese S" first="Silvio" last="Danese">Silvio Danese</name>
<name sortKey="Danese, Silvio" sort="Danese, Silvio" uniqKey="Danese S" first="Silvio" last="Danese">Silvio Danese</name>
<name sortKey="Pansieri, Claudia" sort="Pansieri, Claudia" uniqKey="Pansieri C" first="Claudia" last="Pansieri">Claudia Pansieri</name>
<name sortKey="Pansieri, Claudia" sort="Pansieri, Claudia" uniqKey="Pansieri C" first="Claudia" last="Pansieri">Claudia Pansieri</name>
<name sortKey="Piovani, Daniele" sort="Piovani, Daniele" uniqKey="Piovani D" first="Daniele" last="Piovani">Daniele Piovani</name>
</country>
<country name="France"><region name="Grand Est"><name sortKey="Peyrin Biroulet, Laurent" sort="Peyrin Biroulet, Laurent" uniqKey="Peyrin Biroulet L" first="Laurent" last="Peyrin-Biroulet">Laurent Peyrin-Biroulet</name>
</region>
</country>
</tree>
</affiliations>
</record>
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