Please use this identifier to cite or link to this item: https://doi.org/10.1016/S1473-3099(11)70065-2
Title: Chloroquine for influenza prevention: A randomised, double-blind, placebo controlled trial
Authors: Paton, N.I.
Lee, L.
Xu, Y. 
Ooi, E.E.
Cheung, Y.B. 
Archuleta, S.
Wong, G.
Smith, A.W.
Issue Date: Sep-2011
Citation: Paton, N.I., Lee, L., Xu, Y., Ooi, E.E., Cheung, Y.B., Archuleta, S., Wong, G., Smith, A.W. (2011-09). Chloroquine for influenza prevention: A randomised, double-blind, placebo controlled trial. The Lancet Infectious Diseases 11 (9) : 677-683. ScholarBank@NUS Repository. https://doi.org/10.1016/S1473-3099(11)70065-2
Abstract: Background: Chloroquine has in-vitro activity against influenza and could be an ideal candidate for worldwide prevention of influenza in the period between onset of a pandemic with a virulent influenza strain and the development and widespread dissemination of an effective vaccine. We aimed to assess the efficacy of such an intervention. Methods: In this randomised, double-blind, placebo-controlled trial done at a single centre in Singapore, we randomly assigned (1:1) healthy adults to receive chloroquine phosphate (500 mg/day for 1 week, then once a week to complete 12 weeks) or matching placebo by use of a computer-generated randomisation list. Participants filled an online symptom diary every week, supplemented by daily diaries and self-administered nasal swabs when unwell. Haemagglutination-inhibition assays for influenza A (H1N1, H3N2) and B were done on blood samples taken at baseline and after 12 weeks. The primary outcome was laboratory-confirmed clinical influenza defined by specific symptoms accompanied by influenza RNA on nasal swabs or a four-fold increase in haemagglutination-inhibition titres over the 12-week study period. Analysis was by intention to treat. This trial was registered with ClinicalTrials.gov, number NCT01078779. Findings: From November, 2009, to February, 2010, we recruited 1516 eligible participants. 1496 (96%) returned at week 12 and were included in the efficacy analysis. Adherence to study intervention was 97%, and 94% of the scheduled weekly diaries were completed. Eight (1%) of 738 participants had laboratory-confirmed clinical influenza in the placebo group and 12 (2%) of 724 in the chloroquine group (relative risk 1·53, 95% CI 0·63-3·72; p=0·376). 29 (4%) of 738 had laboratory-confirmed influenza infection (symptomatic or asymptomatic) in the placebo group and 38 (5%) of 724 in the chloroquine group (1·34, 0·83-2·14; p=0·261). 249 (33%) of 759 participants reported adverse events (mostly mild) in the placebo group and 341 (45%) of 757 in chloroquine group (p
Source Title: The Lancet Infectious Diseases
URI: http://scholarbank.nus.edu.sg/handle/10635/109963
ISSN: 14733099
DOI: 10.1016/S1473-3099(11)70065-2
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