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NCT04723446: COVID-19
Efficacy of Mouthwashes in Reducing Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) Viral Load in the Saliva
NA trial testing Corsodyl® Alcohol free -0.2 % Chlorhexidine digluconate in Covid19 in 54 participants. Completed in 25 October 2021.
25 October 2021
Quick facts
| Lead sponsor | Queen Mary University of London |
|---|---|
| Phase | NA |
| Status | Completed |
| Study type | INTERVENTIONAL |
| Allocation | randomized |
| Design | parallel |
| Masking | single |
| Primary purpose | other |
| Enrollment | 54 |
| Start date | 19 May 2021 |
| Primary completion | 25 October 2021 |
| Estimated completion | 25 October 2021 |
| Sites | 2 locations across United Kingdom |
Drugs / interventions tested
- Corsodyl® Alcohol free -0.2 % Chlorhexidine digluconate — full drug profile →
- Colgate Peroxyl® -1.5% Hydrogen peroxide — full drug profile →
- Oral-B® Gum & Enamel Care -Cetylpyridinium chloride
- No rinsing
Conditions studied
- Covid19 — all drugs for Covid19 →
- Coronavirus — all drugs for Coronavirus →
Sponsor
Queen Mary University of London
Who can join
18 and older, any sex, with Covid19 or Coronavirus. Patients with the condition only — healthy volunteers not accepted.
Sponsor's own description
This is a single-blind, parallel-group, randomized pilot study designed to evaluate and compare the efficacy of 3 different mouthwashes containing 0.2% Chlorhexidine digluconate, 1.5% Hydroxide peroxide or Cetylpyridinium chloride in reducing Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) viral load in the saliva of COVID-19 positive patients at different time-points. A convenient sample of up to 40 COVID-19 positive patients diagnosed via test and/or presenting COVID-19 clinical symptoms will be identified in the inpatients and/or outpatient clinics at the Newham University Hospital and at The Royal London Hospital, Barts Health National Health Service (NHS) Trust, United Kingdom (UK). The study will consist of one visit. Unstimulated saliva samples will be collected from all COVID-19 positive patients before and at 30 minutes, 1, 2, and 3 hours after mouth rinsing (Group 1-3 ) or no rinsing (Group 4). Viral load analysis of saliva samples in the different time-points will be then assessed by Reverse Transcription quantitative PCR (RT- qPCR).
Publications & conference data
1 peer-reviewed publication reference this trial (live from Europe PMC):
-
Efficacy of three antimicrobial mouthwashes in reducing SARS-CoV-2 viral load in the saliva of hospitalized patients: a randomized controlled pilot study.
Perussolo J, Teh MT, Gkranias N, Tiberi S, et al · · 2023 · cited 6× · PMID 37542087 · DOI 10.1038/s41598-023-39308-x
Verify or expand the search:
- PubMed search for NCT04723446
- Europe PMC full search
- ASCO Meeting Library
- ESMO Meeting Library
- bioRxiv preprints
- medRxiv preprints
- Google Scholar
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Other Queen Mary University of London trials
Trials by the same sponsor.
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- NCT06937372 — Delivery and Implementation of a Randomised Crossover Trial on Thrombosis · NA · not yet recruiting
- NCT06600438 — Slow-SPEED UK: A Double-Blind Randomised Feasibility Trial · NA · not yet recruiting
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Verify against primary sources
- ClinicalTrials.gov — authoritative US registry record
- WHO ICTRP — international registry index
- EU Clinical Trials Register
- Sponsor press releases (Google)
- Trial protocol + status: ClinicalTrials.gov NCT04723446 (US National Library of Medicine, public domain)
- Publications: Europe PMC API search by NCT ID, retrieved 10 June 2026
- Drug + disease cross-links: matched in real time against Drug Landscape's normalised drug + company + condition tables
- Sponsor: as reported to ClinicalTrials.gov by Queen Mary University of London
- Last refreshed: 14 September 2023
Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT04723446.
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