Literature DB >> 32734670

Characteristics of Clinical Trials relating to COVID-19 registered at ClinicalTrials.gov.

Yuhui Wang1, Qi Zhou2,3, Mengqi Xu4, Jian Kang1, Yaolong Chen3,5,6,7.   

Abstract

WHAT IS KNOWN AND
OBJECTIVE: Since the beginning of the COVID-19 outbreak in China in December 2019, the epidemic has continued to spread globally. Despite continuous reports of clinical trials being launched, no studies have yet systematically summarized and analysed their characteristics. Our objective is to do this by reviewing trials registered at ClinicalTrials.gov.
METHODS: We searched the ClinicalTrials.gov database and retrieved all clinical trials on COVID-19 registered up to and including 3 April 2020. We summarized the characteristics of the trials, presenting the results of all trials, all intervention trials and drug intervention (including vaccines and traditional Chinese medicine) trials. RESULTS AND DISCUSSION: We identified 306 COVID-19-related clinical trials. Seven of the studies had been withdrawn, leaving 299 active trials. Of the trials, 28.8% were planned to be conducted in Asia, 26.8% in Europe and 18.7% in North America. Most (73.0%) proposed trials expected to recruit fewer than 500 people, and only 22.1% of the studies included children (aged <18 years). About two-thirds (67.2%) of the studies were funded by the own resources of medical or research institutions. Of intervention trials, 73.9% used random allocation, and 73.4% used parallel assignment. Only 36.7% of the intervention trials used blinding. In terms of drug trials, 147 trials were drug intervention studies, covering 80 conventional drugs and seven traditional Chinese medicine drugs. Antiviral drugs and antimalarial drugs were the most commonly studied drugs with 52 and 45 trials registered, respectively. Five registered clinical trials were on vaccines. WHAT IS NEW AND
CONCLUSION: A large number of COVID-19-related trials have been registered within the first 4 months since the first infection was reported. These involve a large number of different drugs, the most common being antiviral drugs and antimalarial drugs. More attention should be paid to adequate blinding in future trials.
© 2020 John Wiley & Sons Ltd.

Entities:  

Keywords:  COVID-19; SARS-CoV-2; characteristics analysis; clinical trial registration

Year:  2020        PMID: 32734670     DOI: 10.1111/jcpt.13222

Source DB:  PubMed          Journal:  J Clin Pharm Ther        ISSN: 0269-4727            Impact factor:   2.512


  4 in total

1.  Characteristics analysis for clinical study design relating to COVID-19 based on the database of ClinicalTrials.gov.

Authors:  Hanting Wu; Rongchen Dai; Peijie He; Juan Liang; Qiushuang Li; Junchao Yang; Hanti Lu; Qing Guo; Wei Mao; Conghua Ji
Journal:  Int J Infect Dis       Date:  2022-01-10       Impact factor: 12.074

2.  Funding Sources of Therapeutic and Vaccine Clinical Trials for COVID-19 vs Non-COVID-19 Indications, 2020-2021.

Authors:  Aris Angelis; Carlos Suarez Alonso; Ilias Kyriopoulos; Elias Mossialos
Journal:  JAMA Netw Open       Date:  2022-08-01

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

Authors:  Zhe He; Arslan Erdengasileng; Xiao Luo; Aiwen Xing; Neil Charness; Jiang Bian
Journal:  JAMIA Open       Date:  2021-04-20

4.  How informative were early SARS-CoV-2 treatment and prevention trials? a longitudinal cohort analysis of trials registered on ClinicalTrials.gov.

Authors:  Nora Hutchinson; Katarzyna Klas; Benjamin G Carlisle; Jonathan Kimmelman; Marcin Waligora
Journal:  PLoS One       Date:  2022-01-21       Impact factor: 3.240

  4 in total

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