Serveur d'exploration COVID et hydrochloroquine

Attention, ce site est en cours de développement !
Attention, site généré par des moyens informatiques à partir de corpus bruts.
Les informations ne sont donc pas validées.

How the clinical research community responded to the COVID-19 pandemic: An analysis of the COVID-19 clinical studies in ClinicalTrials.gov.

Identifieur interne : 000B26 ( Main/Corpus ); précédent : 000B25; suivant : 000B27

How the clinical research community responded to the COVID-19 pandemic: An analysis of the COVID-19 clinical studies in ClinicalTrials.gov.

Auteurs : Zhe He ; Fnu Erdengasileng ; Xiao Luo ; Aiwen Xing ; Neil Charness ; Jiang Bian

Source :

RBID : pubmed:32995807

Abstract

OBJECTIVE

The novel coronavirus disease (COVID-19), broke out in December 2019, is a global pandemic. Rapidly in the past few months, a large number of clinical studies have been initiated worldwide to find effective therapeutics, vaccines, and preventive strategies. In this study, we aim to understand the landscape of COVID-19 clinical research and identify the gaps and issues that may cause difficulty in recruitment and the lack of population representativeness.

MATERIALS AND METHODS

We analyzed 2,034 COVID-19 studies registered in the largest public registry - ClinicalTrials.gov. Leveraging natural language processing, descriptive analysis, association analysis, and clustering analysis, we characterized COVID-19 clinical studies by phase and design features. Particularly, we analyzed their eligibility criteria to understand: (1) whether they considered the reported underlying health conditions that may lead to severe illnesses, and (2) if these studies excluded older adults, either explicitly or implicitly, which may reduce the generalizability of these studies in older adults.

RESULTS

The 5 most frequently tested drugs are Hydroxychloroquine (N=148), Azithromycin (N=46), Tocilizumab (N=29), Lopinavir (N=20), and Ritonavir (N=20). Most trials did not have an upper age limit and did not exclude patients with common chronic conditions such as hypertension and diabetes that are prevalent in older adults. However, known risk factors that may lead to severe illnesses have not been adequately considered by existing studies.

CONCLUSIONS

A careful examination of the registered COVID-19 clinical studies can identify the research gaps and inform future COVID-19 trial design towards balanced internal validity and generalizability.


DOI: 10.1101/2020.09.16.20195552
PubMed: 32995807
PubMed Central: PMC7523146

Links to Exploration step

pubmed:32995807

Le document en format XML

<record>
<TEI>
<teiHeader>
<fileDesc>
<titleStmt>
<title xml:lang="en">How the clinical research community responded to the COVID-19 pandemic: An analysis of the COVID-19 clinical studies in ClinicalTrials.gov.</title>
<author>
<name sortKey="He, Zhe" sort="He, Zhe" uniqKey="He Z" first="Zhe" last="He">Zhe He</name>
</author>
<author>
<name sortKey="Erdengasileng, Fnu" sort="Erdengasileng, Fnu" uniqKey="Erdengasileng F" first="Fnu" last="Erdengasileng">Fnu Erdengasileng</name>
</author>
<author>
<name sortKey="Luo, Xiao" sort="Luo, Xiao" uniqKey="Luo X" first="Xiao" last="Luo">Xiao Luo</name>
</author>
<author>
<name sortKey="Xing, Aiwen" sort="Xing, Aiwen" uniqKey="Xing A" first="Aiwen" last="Xing">Aiwen Xing</name>
</author>
<author>
<name sortKey="Charness, Neil" sort="Charness, Neil" uniqKey="Charness N" first="Neil" last="Charness">Neil Charness</name>
</author>
<author>
<name sortKey="Bian, Jiang" sort="Bian, Jiang" uniqKey="Bian J" first="Jiang" last="Bian">Jiang Bian</name>
</author>
</titleStmt>
<publicationStmt>
<idno type="wicri:source">PubMed</idno>
<date when="2020">2020</date>
<idno type="RBID">pubmed:32995807</idno>
<idno type="pmid">32995807</idno>
<idno type="doi">10.1101/2020.09.16.20195552</idno>
<idno type="pmc">PMC7523146</idno>
<idno type="wicri:Area/Main/Corpus">000B26</idno>
<idno type="wicri:explorRef" wicri:stream="Main" wicri:step="Corpus" wicri:corpus="PubMed">000B26</idno>
</publicationStmt>
<sourceDesc>
<biblStruct>
<analytic>
<title xml:lang="en">How the clinical research community responded to the COVID-19 pandemic: An analysis of the COVID-19 clinical studies in ClinicalTrials.gov.</title>
<author>
<name sortKey="He, Zhe" sort="He, Zhe" uniqKey="He Z" first="Zhe" last="He">Zhe He</name>
</author>
<author>
<name sortKey="Erdengasileng, Fnu" sort="Erdengasileng, Fnu" uniqKey="Erdengasileng F" first="Fnu" last="Erdengasileng">Fnu Erdengasileng</name>
</author>
<author>
<name sortKey="Luo, Xiao" sort="Luo, Xiao" uniqKey="Luo X" first="Xiao" last="Luo">Xiao Luo</name>
</author>
<author>
<name sortKey="Xing, Aiwen" sort="Xing, Aiwen" uniqKey="Xing A" first="Aiwen" last="Xing">Aiwen Xing</name>
</author>
<author>
<name sortKey="Charness, Neil" sort="Charness, Neil" uniqKey="Charness N" first="Neil" last="Charness">Neil Charness</name>
</author>
<author>
<name sortKey="Bian, Jiang" sort="Bian, Jiang" uniqKey="Bian J" first="Jiang" last="Bian">Jiang Bian</name>
</author>
</analytic>
<series>
<title level="j">medRxiv : the preprint server for health sciences</title>
<imprint>
<date when="2020" type="published">2020</date>
</imprint>
</series>
</biblStruct>
</sourceDesc>
</fileDesc>
<profileDesc>
<textClass></textClass>
</profileDesc>
</teiHeader>
<front>
<div type="abstract" xml:lang="en">
<p>
<b>OBJECTIVE</b>
</p>
<p>The novel coronavirus disease (COVID-19), broke out in December 2019, is a global pandemic. Rapidly in the past few months, a large number of clinical studies have been initiated worldwide to find effective therapeutics, vaccines, and preventive strategies. In this study, we aim to understand the landscape of COVID-19 clinical research and identify the gaps and issues that may cause difficulty in recruitment and the lack of population representativeness.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>MATERIALS AND METHODS</b>
</p>
<p>We analyzed 2,034 COVID-19 studies registered in the largest public registry - ClinicalTrials.gov. Leveraging natural language processing, descriptive analysis, association analysis, and clustering analysis, we characterized COVID-19 clinical studies by phase and design features. Particularly, we analyzed their eligibility criteria to understand: (1) whether they considered the reported underlying health conditions that may lead to severe illnesses, and (2) if these studies excluded older adults, either explicitly or implicitly, which may reduce the generalizability of these studies in older adults.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>RESULTS</b>
</p>
<p>The 5 most frequently tested drugs are Hydroxychloroquine (N=148), Azithromycin (N=46), Tocilizumab (N=29), Lopinavir (N=20), and Ritonavir (N=20). Most trials did not have an upper age limit and did not exclude patients with common chronic conditions such as hypertension and diabetes that are prevalent in older adults. However, known risk factors that may lead to severe illnesses have not been adequately considered by existing studies.</p>
</div>
<div type="abstract" xml:lang="en">
<p>
<b>CONCLUSIONS</b>
</p>
<p>A careful examination of the registered COVID-19 clinical studies can identify the research gaps and inform future COVID-19 trial design towards balanced internal validity and generalizability.</p>
</div>
</front>
</TEI>
<pubmed>
<MedlineCitation Status="PubMed-not-MEDLINE" Owner="NLM">
<PMID Version="1">32995807</PMID>
<DateRevised>
<Year>2020</Year>
<Month>12</Month>
<Day>29</Day>
</DateRevised>
<Article PubModel="Electronic">
<Journal>
<JournalIssue CitedMedium="Internet">
<PubDate>
<Year>2020</Year>
<Month>Sep</Month>
<Day>19</Day>
</PubDate>
</JournalIssue>
<Title>medRxiv : the preprint server for health sciences</Title>
<ISOAbbreviation>medRxiv</ISOAbbreviation>
</Journal>
<ArticleTitle>How the clinical research community responded to the COVID-19 pandemic: An analysis of the COVID-19 clinical studies in ClinicalTrials.gov.</ArticleTitle>
<ELocationID EIdType="pii" ValidYN="Y">2020.09.16.20195552</ELocationID>
<ELocationID EIdType="doi" ValidYN="Y">10.1101/2020.09.16.20195552</ELocationID>
<Abstract>
<AbstractText Label="OBJECTIVE" NlmCategory="OBJECTIVE">The novel coronavirus disease (COVID-19), broke out in December 2019, is a global pandemic. Rapidly in the past few months, a large number of clinical studies have been initiated worldwide to find effective therapeutics, vaccines, and preventive strategies. In this study, we aim to understand the landscape of COVID-19 clinical research and identify the gaps and issues that may cause difficulty in recruitment and the lack of population representativeness.</AbstractText>
<AbstractText Label="MATERIALS AND METHODS" NlmCategory="METHODS">We analyzed 2,034 COVID-19 studies registered in the largest public registry - ClinicalTrials.gov. Leveraging natural language processing, descriptive analysis, association analysis, and clustering analysis, we characterized COVID-19 clinical studies by phase and design features. Particularly, we analyzed their eligibility criteria to understand: (1) whether they considered the reported underlying health conditions that may lead to severe illnesses, and (2) if these studies excluded older adults, either explicitly or implicitly, which may reduce the generalizability of these studies in older adults.</AbstractText>
<AbstractText Label="RESULTS" NlmCategory="RESULTS">The 5 most frequently tested drugs are Hydroxychloroquine (N=148), Azithromycin (N=46), Tocilizumab (N=29), Lopinavir (N=20), and Ritonavir (N=20). Most trials did not have an upper age limit and did not exclude patients with common chronic conditions such as hypertension and diabetes that are prevalent in older adults. However, known risk factors that may lead to severe illnesses have not been adequately considered by existing studies.</AbstractText>
<AbstractText Label="CONCLUSIONS" NlmCategory="CONCLUSIONS">A careful examination of the registered COVID-19 clinical studies can identify the research gaps and inform future COVID-19 trial design towards balanced internal validity and generalizability.</AbstractText>
</Abstract>
<AuthorList CompleteYN="Y">
<Author ValidYN="Y">
<LastName>He</LastName>
<ForeName>Zhe</ForeName>
<Initials>Z</Initials>
<Identifier Source="ORCID">0000-0003-3608-0244</Identifier>
</Author>
<Author ValidYN="Y">
<LastName>Erdengasileng</LastName>
<ForeName>Fnu</ForeName>
<Initials>F</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Luo</LastName>
<ForeName>Xiao</ForeName>
<Initials>X</Initials>
<Identifier Source="ORCID">0000-0002-3649-9785</Identifier>
</Author>
<Author ValidYN="Y">
<LastName>Xing</LastName>
<ForeName>Aiwen</ForeName>
<Initials>A</Initials>
<Identifier Source="ORCID">0000-0003-4901-7025</Identifier>
</Author>
<Author ValidYN="Y">
<LastName>Charness</LastName>
<ForeName>Neil</ForeName>
<Initials>N</Initials>
</Author>
<Author ValidYN="Y">
<LastName>Bian</LastName>
<ForeName>Jiang</ForeName>
<Initials>J</Initials>
<Identifier Source="ORCID">0000-0002-2238-5429</Identifier>
</Author>
</AuthorList>
<Language>eng</Language>
<GrantList CompleteYN="Y">
<Grant>
<GrantID>R21 AG061431</GrantID>
<Acronym>AG</Acronym>
<Agency>NIA NIH HHS</Agency>
<Country>United States</Country>
</Grant>
<Grant>
<GrantID>UL1 TR001427</GrantID>
<Acronym>TR</Acronym>
<Agency>NCATS NIH HHS</Agency>
<Country>United States</Country>
</Grant>
</GrantList>
<PublicationTypeList>
<PublicationType UI="D000076942">Preprint</PublicationType>
</PublicationTypeList>
<ArticleDate DateType="Electronic">
<Year>2020</Year>
<Month>09</Month>
<Day>19</Day>
</ArticleDate>
</Article>
<MedlineJournalInfo>
<Country>United States</Country>
<MedlineTA>medRxiv</MedlineTA>
<NlmUniqueID>101767986</NlmUniqueID>
</MedlineJournalInfo>
</MedlineCitation>
<PubmedData>
<History>
<PubMedPubDate PubStatus="entrez">
<Year>2020</Year>
<Month>9</Month>
<Day>30</Day>
<Hour>6</Hour>
<Minute>16</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="pubmed">
<Year>2020</Year>
<Month>10</Month>
<Day>1</Day>
<Hour>6</Hour>
<Minute>0</Minute>
</PubMedPubDate>
<PubMedPubDate PubStatus="medline">
<Year>2020</Year>
<Month>10</Month>
<Day>1</Day>
<Hour>6</Hour>
<Minute>1</Minute>
</PubMedPubDate>
</History>
<PublicationStatus>epublish</PublicationStatus>
<ArticleIdList>
<ArticleId IdType="pubmed">32995807</ArticleId>
<ArticleId IdType="doi">10.1101/2020.09.16.20195552</ArticleId>
<ArticleId IdType="pmc">PMC7523146</ArticleId>
</ArticleIdList>
<ReferenceList>
<Reference>
<Citation>JAMA Intern Med. 2020 Oct 1;180(10):1398-1400</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32730617</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>PLoS One. 2020 Sep 30;15(9):e0239694</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32997699</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Front Pharmacol. 2020 Sep 02;11:540187</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32982751</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>J Infect. 2020 Aug;81(2):e16-e25</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32335169</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Clin Microbiol Infect. 2020 Aug;26(8):988-998</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32454187</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>J Med Internet Res. 2018 Apr 12;20(4):e137</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">29650502</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>J Transl Med. 2020 Jul 6;18(1):274</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32631442</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>JAMA. 2020 Jun 23;323(24):2455-2457</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32421150</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>AMIA Annu Symp Proc. 2018 Apr 16;2017:849-858</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">29854151</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>J Clin Epidemiol. 2020 Sep;125:170-178</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32526460</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>NPJ Digit Med. 2020 Jul 31;3:101</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32821856</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>J Clin Pharm Ther. 2020 Dec;45(6):1357-1362</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32734670</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>BMJ Open. 2020 Sep 17;10(9):e041276</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32948577</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>J Am Med Inform Assoc. 2020 Dec 01;:</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">33260201</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Sao Paulo Med J. 2020 Sep-Oct;138(5):441-456</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32813843</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Nature. 2020 Dec;588(7837):205-206</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">33288887</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>PLoS One. 2020 Oct 6;15(10):e0240123</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">33022014</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Ann Intern Med. 2016 Sep 20;165(6):421-30</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">27294570</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Nat Med. 2020 Aug;26(8):1205-1211</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32546824</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Clin Transl Sci. 2020 Jul;13(4):675-684</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32058639</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>BMC Med. 2020 Jun 1;18(1):167</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32493331</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Methods Inf Med. 2016 May 17;55(3):266-75</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">26940748</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>Stroke. 2006 Jan;37(1):209-15</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">16339480</ArticleId>
</ArticleIdList>
</Reference>
<Reference>
<Citation>J Reprod Immunol. 2020 Jun;139:103122</Citation>
<ArticleIdList>
<ArticleId IdType="pubmed">32244166</ArticleId>
</ArticleIdList>
</Reference>
</ReferenceList>
</PubmedData>
</pubmed>
</record>

Pour manipuler ce document sous Unix (Dilib)

EXPLOR_STEP=$WICRI_ROOT/Sante/explor/CovidChloroV1/Data/Main/Corpus
HfdSelect -h $EXPLOR_STEP/biblio.hfd -nk 000B26 | SxmlIndent | more

Ou

HfdSelect -h $EXPLOR_AREA/Data/Main/Corpus/biblio.hfd -nk 000B26 | SxmlIndent | more

Pour mettre un lien sur cette page dans le réseau Wicri

{{Explor lien
   |wiki=    Sante
   |area=    CovidChloroV1
   |flux=    Main
   |étape=   Corpus
   |type=    RBID
   |clé=     pubmed:32995807
   |texte=   How the clinical research community responded to the COVID-19 pandemic: An analysis of the COVID-19 clinical studies in ClinicalTrials.gov.
}}

Pour générer des pages wiki

HfdIndexSelect -h $EXPLOR_AREA/Data/Main/Corpus/RBID.i   -Sk "pubmed:32995807" \
       | HfdSelect -Kh $EXPLOR_AREA/Data/Main/Corpus/biblio.hfd   \
       | NlmPubMed2Wicri -a CovidChloroV1 

Wicri

This area was generated with Dilib version V0.6.38.
Data generation: Sat May 22 17:02:32 2021. Site generation: Sat May 22 17:06:52 2021