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Ivermectin for COVID-19 in adults in the community (PRINCIPLE): An open, randomised, controlled, adaptive platform trial of short- and longer-term outcomes.
Hayward, Gail; Yu, Ly-Mee; Little, Paul; Gbinigie, Oghenekome; Shanyinde, Milensu; Harris, Victoria; Dorward, Jienchi; Saville, Benjamin R; Berry, Nicholas; Evans, Philip H; Thomas, Nicholas P B; Patel, Mahendra G; Richards, Duncan; Hecke, Oliver V; Detry, Michelle A; Saunders, Christina; Fitzgerald, Mark; Robinson, Jared; Latimer-Bell, Charlotte; Allen, Julie; Ogburn, Emma; Grabey, Jenna; de Lusignan, Simon; Hobbs, Fd Richard; Butler, Christopher C.
Afiliação
  • Hayward G; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Yu LM; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Little P; Primary Care Research Centre, University of Southampton, Southampton, UK.
  • Gbinigie O; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Shanyinde M; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Harris V; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Dorward J; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK; Centre for the AIDS Programme of Research in South Africa (CAPRISA), University of KwaZulu-Natal, Durban, South Africa.
  • Saville BR; Berry Consultants, TX, USA; Department of Biostatistics, Vanderbilt University School of Medicine, TN, USA.
  • Berry N; Berry Consultants, TX, USA.
  • Evans PH; College of Medicine and Health, University of Exeter, Exeter, UK; National Institute for Health Research (NIHR) Clinical Research Network, National Institute for Health Research, London, UK.
  • Thomas NPB; National Institute for Health Research (NIHR) Clinical Research Network, National Institute for Health Research, London, UK.
  • Patel MG; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Richards D; Royal College of General Practitioners, London, UK; Oxford Clinical Trials Research Unit, Botnar Research Centre, University of Oxford, Oxford, UK.
  • Hecke OV; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Detry MA; Berry Consultants, TX, USA.
  • Saunders C; Berry Consultants, TX, USA.
  • Fitzgerald M; Berry Consultants, TX, USA.
  • Robinson J; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Latimer-Bell C; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Allen J; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Ogburn E; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Grabey J; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • de Lusignan S; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.
  • Hobbs FR; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK. Electronic address: principle@phc.ox.ac.uk.
  • Butler CC; Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK. Electronic address: principle@phc.ox.ac.uk.
J Infect ; 88(4): 106130, 2024 Apr.
Article em En | MEDLINE | ID: mdl-38431155
ABSTRACT

BACKGROUND:

The evidence for whether ivermectin impacts recovery, hospital admissions, and longer-term outcomes in COVID-19 is contested. The WHO recommends its use only in the context of clinical trials.

METHODS:

In this multicentre, open-label, multi-arm, adaptive platform randomised controlled trial, we included participants aged ≥18 years in the community, with a positive SARS-CoV-2 test, and symptoms lasting ≤14 days. Participants were randomised to usual care, usual care plus ivermectin tablets (target 300-400 µg/kg per dose, once daily for 3 days), or usual care plus other interventions. Co-primary endpoints were time to first self-reported recovery, and COVID-19 related hospitalisation/death within 28 days, analysed using Bayesian models. Recovery at 6 months was the primary, longer term outcome. TRIAL REGISTRATION ISRCTN86534580.

FINDINGS:

The primary analysis included 8811 SARS-CoV-2 positive participants (median symptom duration 5 days), randomised to ivermectin (n = 2157), usual care (n = 3256), and other treatments (n = 3398) from June 23, 2021 to July 1, 2022. Time to self-reported recovery was shorter in the ivermectin group compared with usual care (hazard ratio 1·15 [95% Bayesian credible interval, 1·07 to 1·23], median decrease 2.06 days [1·00 to 3·06]), probability of meaningful effect (pre-specified hazard ratio ≥1.2) 0·192). COVID-19-related hospitalisations/deaths (odds ratio 1·02 [0·63 to 1·62]; estimated percentage difference 0% [-1% to 0·6%]), serious adverse events (three and five respectively), and the proportion feeling fully recovered were similar in both groups at 6 months (74·3% and 71·2% respectively (RR = 1·05, [1·02 to 1·08]) and also at 3 and 12 months.

INTERPRETATION:

Ivermectin for COVID-19 is unlikely to provide clinically meaningful improvement in recovery, hospital admissions, or longer-term outcomes. Further trials of ivermectin for SARS-Cov-2 infection in vaccinated community populations appear unwarranted.

FUNDING:

UKRI/National Institute of Health Research (MC_PC_19079).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: COVID-19 Limite: Adolescent / Adult / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: COVID-19 Limite: Adolescent / Adult / Humans Idioma: En Ano de publicação: 2024 Tipo de documento: Article