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Clinical investigation of the effectiveness of different mouth rinses in Covid-19-Patients

Conditions
COVID-19
Registration Number
DRKS00023725
Lead Sponsor
niversität Witten/Herdecke Fakultät für Gesundheit (Department für Zahn-, Mund- und Kieferheilkunde)Lehrstuhl für Zahnerhaltung und Präventive Zahnmedizin
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
60
Inclusion Criteria

Age: 18-80 years
- Positive, confirmed disease with Covid-19
- Good general condition of the patient
- No elevated temperature
- No elevated blood pressure/pulse
- No increased respiratory rate
- No medication intake
- Presentation of the consent form of the Subject

Exclusion Criteria

- severe general illness
- Subjects with physical and/or mental disabilities mental disabilities with limited manual and cognitive abilities and therefore no comparability possible
- Allergic reactions to the substances used in the study (e.g. hydrogen peroxide)
- alcohol abuse
- Lack of compliance, so that it cannot be ensured that the patients* comply with the study protocol.
- Pregnancy and lactation

Study & Design

Study Type
observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
The aim of this study is to determine the virus detection in the throat, using polymerase chain reaction (PCR), in SARS-CoV-2 patients after using the four different mouthwashes with different concentrations and residence time in the mouth.
Secondary Outcome Measures
NameTimeMethod
The second goal is to find out a correlation of the viral load, between the saliva-NaCl mixture (rinsing with NaCl) and the throat swab.
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