Abstract: medRxiv preprint doi: https://doi.org/10.1101/2020.11.27.20234997; this version posted April 25, 2021. The copyright holder for this preprint
(which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity.
It is made available under a CC-BY-NC-ND 4.0 International license .
Title:
A randomized trial on the regular use of potent mouthwash in COVID-19 treatment
Authors list:
Khalid Mukhtar 1 (First & corresponding Author), kmukhter@hamad.qa
Suelen Qassim 2, sq1513914@student.qu.edu.qa
Shaikha Ali Al Qahtani 3, SALQAHTANI4@hamad.qa
Mohamed Ibn-Masud Danjuma 4, mdanjuma@hamad.qa
Mohamed Mohamedali 5, mmohamedali@hamad.qa
Housamaddeen Al Farhan 6, halfarhan1@hamad.qa
Mohammed F. Khudair 7, mkhudhair@hamad.qa
Abdel Rehim El Tayeh 8, aeltayeh@hamad.qa
Mohammed Al-Dosari 9, maldosari1@hamad.qa
Mohamed Elhassan Babiker 10, mbabiker@hamad.qa
Ahmed Hassib 11, ahassib1@hamad.qa
Rumaisa Mohamed Elmustafa 12, rmohamed31@hamad.qa
Wesal Elhadary 13, welhadary@hamad.qa
Morwan Abdulkarim 14, mabdulkrim@hamad.qa
Rajvir Singh 15, rsingh@hamad.qa
Muna Al.Maslamani 16, malmaslamani@hamad.qa
Authors affiliation:
Hamad Medical Corporation, Doha, QATAR (1, 3, 4, 5, 6, 7, 8,9, 10, 11, 12, 13, 14, 15, 16)
Qatar University – Public Health program, Doha, Qatar (2)
NOTE: This preprint reports new research that has not been certified by peer review and should not be used to guide clinical practice.
medRxiv preprint doi: https://doi.org/10.1101/2020.11.27.20234997; this version posted April 25, 2021. The copyright holder for this preprint
(which was not certified by peer review) is the author/funder, who has granted medRxiv a license to display the preprint in perpetuity.
It is made available under a CC-BY-NC-ND 4.0 International license .
1. Abstract
In this work we tried to study the effect of the regular use of potent mouthwash in COVID19 cases,
on the premise that it may speedup the recovery, through the repeated reduction of microbial load,
of both, the 2019-nCOV and oral microbiota; thus slowing the disease progression and lowering the
incidence of superinfections.
Through a randomized controlled trial, a mixed solution of Hydrogen peroxide 2% and
chlorhexidine gluconate, to be used for oral rinsing and gargling three times daily, was tested in
cases admitted to COVID treatment facility, versus the standard (only) COVID19-treatment
protocol, starting with 46 cases in each group, matched in terms of disease severity, of symptoms,
and average cycle threshold value (CT-value) for the COVID PCR test on diagnosis.
Our findings showed statistically significant improvement in terms of a higher conversion rate to
"COVID19-negative PCR" by five days of treatment (6/46 Vs 0/46), improvement in “symptoms
severity” after two days of treatment, and less intubation and mortality (0/46 Vs 3/46) with all Pvalue < 0.05. There was also a trend of improvement in other outcome variables, though with no
statistically significant difference; namely “shorter hospital stays," "less progression in Oxygen
requirements”, “less rate of plasma transfusion”, and better "gross extent of improvement”.
Our findings support a beneficial role in treating active cases (Disease) and anticipates better
outcome should implemented earlier in course of the disease; thus, suggest a role in limiting the
spread (Pandemic), as an additional preventive method. Additionally, we think the repeated
reduction in the microbial load..
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'abstract': '<jats:label>1.</jats:label><jats:title>Abstract</jats:title><jats:p>In this work we tried to '
'study the effect of the regular use of potent mouthwash in COVID19 cases, on the premise that '
'it may speedup the recovery, through the repeated reduction of microbial load, of both, the '
'2019-nCOV and oral microbiota; thus slowing the disease progression and lowering the '
'incidence of superinfections.</jats:p><jats:p>Through a randomized controlled trial, a mixed '
'solution of Hydrogen peroxide 2% and chlorhexidine gluconate, to be used for oral rinsing and '
'gargling three times daily, was tested in cases admitted to COVID treatment facility, versus '
'the standard (only) COVID19-treatment protocol, starting with 46 cases in each group, matched '
'in terms of disease severity, of symptoms, and average cycle threshold value (CT-value) for '
'the COVID PCR test on diagnosis.</jats:p><jats:p>Our findings showed statistically '
'significant improvement in terms of a higher conversion rate to “COVID19-negative PCR” by '
'five days of treatment (6/46 Vs 0/46), improvement in “symptoms severity” after two days of '
'treatment, and less intubation and mortality (0/46 Vs 3/46) with all P-value < 0.05. There '
'was also a trend of improvement in other outcome variables, though with no statistically '
'significant difference; namely “shorter hospital stays,” “less progression in Oxygen '
'requirements”, “less rate of plasma transfusion”, and better “gross extent of '
'improvement”.</jats:p><jats:p>Our findings support a beneficial role in treating active cases '
'(Disease) and anticipates better outcome should implemented earlier in course of the disease; '
'thus, suggest a role in limiting the spread (Pandemic), as an additional preventive method. '
'Additionally, we think the repeated reduction in the microbial load might have been '
'sufficient to induce a strain in a possible viral-microbial interaction, resulting in slowing '
'down of the disease progress.</jats:p>',
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