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Measurement of the effect of mouthwash against COVID-19

Measurement of mouthwash anti-viral activity against COVID-19 (MOMA)

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ISRCTN
Registry ID
ISRCTN25647404
Enrollment
104
Registered
2020-11-09
Start date
2020-09-20
Completion date
Unknown
Last updated
2026-02-09

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

COVID-19 (SARS-CoV-2 infection) Infections and Infestations

Interventions

The study consists of a single treatment with no follow-up. Participants will be assigned to one of the four arms using a balanced randomisation scheme: Dentyl Mouthwash (Cetylperidium chloride 0.05%
povidone-iodine (PVP-I 0.5% [v/v])
Ultradex (Cetylperidium chloride 0.1% [v/v]) or Normasol (sterile saline 0.9% [v/v]). The three test (active) agents will all be used according to their current marketing approval. Baseline saliva wil

Sponsors

Cardiff University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 100 Years

Inclusion criteria

Inclusion criteria: Eligible patients will be approached and recruited from COVID in-patient wards within Cardiff and Vale University Health Board, Betsi Cadwaladr University Health Board, University Hospitals Bristol NHS Foundation Trust and Cwm Taf Morganwg University Health Board. Only patients who are deemed well enough and able to provide informed consent by their local clinical teams will be approached to take part in the study. Specific inclusion criteria are: 1. Adults aged =18 years 2. With positive SARS-CoV-2 carriage by RT-PCR within 14 days 3. Capable of using the mouthwash required by the trial 4. Capacity and capability to give informed consent to take part in the trial

Exclusion criteria

Exclusion criteria: 1. Known or suspected intolerance or hypersensitivity to povidone-iodine or other study materials (or closely related compounds) or any of their stated ingredients 2. Known pregnancy, currently breastfeeding or women of childbearing age without effective contraception 3. Current requirement for invasive or non-invasive ventilation; or planned within next 6 hours 4. Known dermatitis herpetiformis (Duhring's disease) 5. Inability to communicate in English or read English

Design outcomes

Primary

MeasureTime frame
Viral load of SARS CoV-2 measured by in vitro culture and confirmed by RT-qPCR at 30 minutes

Secondary

MeasureTime frame
Viral load of SARS CoV-2 measured by in vitro culture and confirmed by RT-qPCR at baseline and then after 1, 15 and 60 minutes

Countries

England, United Kingdom, Wales

Contacts

Public ContactDavid Thomas
thomasdw2@cardiff.ac.uk+44 (0)2920742416

Outcome results

None listed

Source: ISRCTN (via WHO ICTRP) · Data processed: Feb 13, 2026