4.7 Article

Use of an antiviral mouthwash as a barrier measure in the SARS-CoV-2 transmission in adults with asymptomatic to mild COVID-19: a multicentre, randomized, double-blind controlled trial

Journal

CLINICAL MICROBIOLOGY AND INFECTION
Volume 27, Issue 10, Pages 1494-1501

Publisher

ELSEVIER SCI LTD
DOI: 10.1016/j.cmi.2021.05.028

Keywords

beta-cyclodextrin; Citrox; Coronavirus disease 2019; Mouthwash; Saliva; Severe acute respiratory syndrome coronavirus 2; Viral load

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The commercially available mouthwash with beta-cyclodextrin and citrox can effectively reduce the salivary viral load of SARS-CoV-2, showing significant short-term and long-term benefits over the placebo group on day 1 and day 7 respectively.
Objectives: To determine if commercially available mouthwash with beta-cyclodextrin and citrox (bioflavonoids) (CDCM) could decrease the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) salivary viral load. Methods: In this randomized controlled trial, severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) PCR-positive patients aged 18-85 years with asymptomatic to mild coronavirus disease 2019 (COVID-19) symptoms for <8 days were recruited. A total of 176 eligible patients were randomly assigned (1:1) to CDCM or placebo. Three rinses daily were performed for 7 days. Saliva sampling was performed on day 1 at 09.00 (T1), 13.00 (T2) and 18.00 (T3). On the following 6 days, one sample was taken at 15.00. Quantitative RT-PCR was used to detect SARS-CoV-2. Results: The intention-to-treat analysis demonstrated that, over the course of 1 day, CDCM was significantly more effective than placebo 4 hours after the first dose (p 0.036), with a median percentage (log(10) copies/mL) decrease T1-T2 of-12.58% (IQR-29.55% to-0.16%). The second dose maintained the low median value for the CDCM (3.08 log(10) copies/mL; IQR 0-4.19), compared with placebo (3.31 log(10) copies/mL; IQR 1.18-4.75). At day 7, there was still a greater median percentage (log(10) copies/mL) decrease in salivary viral load over time in the CDCM group (-58.62%; IQR-100% to-34.36%) compared with the placebo group (-50.62%; IQR-100% to-27.66%). These results were confirmed by the per-protocol analysis. Conclusions: This trial supports the relevance of using CDCM on day 1 (4 hours after the initial dose) to reduce the SARS-CoV-2 viral load in saliva. For long-term effect (7 days), CDMC appears to provide a modest benefit compared with placebo in reducing viral load in saliva. (C) 2021 The Author(s). Published by Elsevier Ltd on behalf of European Society of Clinical Microbiology and Infectious Diseases.

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