Effect of mouthwash on the reduction of salivary SARS-CoV-2
- Conditions
- COVID-19
- Registration Number
- JPRN-jRCTs031230566
- Lead Sponsor
- Kutsuna Satoshi
- Brief Summary
Not available
- Detailed Description
Not available
Recruitment & Eligibility
- Status
- Recruiting
- Sex
- All
- Target Recruitment
- 66
(1) Person who is diagnosed with COVID-19 using nucleic acid amplification method (PCR method, LAMP method, etc.), antigen qualitative test, antigen quantitative test
(2) Person with mild severity class ification in the medical guide for COVID-19 (version 10.0) at informed consent
(3) Person who is scheduled to have the day of mouthwash within 3 days from the symptom onset date (or the sample collection date for positive confirmation when asymptomatic or the onset date is not clear)
(4) Aged 18 years or older at informed consent
(5) Person who has written consent to participate in this study
(1) Person who has difficulty collecting saliva by him/herself due to the effects of old age, Sjogren's syndrome, radiation therapy for malignant tumors, etc.
(2) Person who received or is scheduled to receive remdesivir, molnupiravir, nilmatrelvir / ritnavir, Ensitrelvir,sotrovimab, casilibimab / imdebimab,Tixagevimab/Cilgavimab after the onset of this COVID-19
(3) Person who received anti-IL-6 antibody (tocilizumab, etc.), JAK inhibitors (baricitinib, etc.), oral
or injectable steroids within the past 2 weeks, or will be administered by the morning of the day of mouthwash (Including administration for diseases other than COVID-19)
(4) Person who participated in clinical trials of COVID-19 therapeutic agents since the onset of this
COVID-19
(5) Person with pregnant or lactating
(6) Person with a history of hypersensitivity to the ingredients of Medicinal Mondamin X-9N or A2Car
e Mouthwash
(7) Person who is judged by the investigator to be inappropriate as research subjects for other reaso
ns
Study & Design
- Study Type
- Interventional
- Study Design
- Not specified
- Primary Outcome Measures
Name Time Method
- Secondary Outcome Measures
Name Time Method