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David Hutton

Researcher at University of Bristol

Publications -  5
Citations -  2080

David Hutton is an academic researcher from University of Bristol. The author has contributed to research in topics: Rate ratio & Randomized controlled trial. The author has an hindex of 3, co-authored 5 publications receiving 1011 citations.

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Journal ArticleDOI

Repurposed Antiviral Drugs for Covid-19 - Interim WHO Solidarity Trial Results.

Hongchao Pan, +73 more
TL;DR: These remdesivir, hydroxychloroquine, lopinavir, and interferon regimens had little or no effect on hospitalized patients with Covid-19, as indicated by overall mortality, initiation of ventilation, and duration of hospital stay.
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Safety and immunogenicity of concomitant administration of COVID-19 vaccines (ChAdOx1 or BNT162b2) with seasonal influenza vaccines in adults in the UK (ComFluCOV): a multicentre, randomised, controlled, phase 4 trial.

Rajeka Lazarus, +183 more
- 11 Nov 2021 - 
TL;DR: In this article, the safety of concomitant vaccination with COVID-19 and influenza vaccines was evaluated in a randomized, controlled, phase 4 trial, where participants were randomly assigned to receive either an age-appropriate influenza vaccine or placebo alongside their second dose of COVID19 vaccine.
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Screening for hereditary haemochromatosis within families and beyond.

TL;DR: Overall efficacy of population screening for haemochromatosis is undermined by observations that a substantial number of untested relatives had undiagnosed iron overload.
Journal ArticleDOI

Development of the "GeneSYS" database system to support trial data capture and conduct

TL;DR: Recognising the need to develop flexible database solutions quickly, and that are easily maintained throughout the life cycle of a study, the CTU database development team conceived and developed the “GeneSYS” database solution.
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Improving the efficiency of testing database functionality through statistical involvement

TL;DR: This work describes how, with statistical involvement, the testing has been streamlined and the timelines reduced in customised databases to collect and store study data and manage clinical trials.