Evaluation of SARS-COV-2 Viral Load of Covid-19 Patients After Rinsing With Oral Antimicrobial Mouthwashes

Hospital Israelita Albert Einstein

Status: Completed

Conditions: Covid19

Treatments: Other: CPC; Other: CPC+ZN; Other: Negative Control

Study type: Interventional

Funder types: Other; Industry

Identifiers

NCT04902976

4560-21

Details and patient eligibility

About

The aim of this study is to analyze the efficacy of oral disinfection with 0.075% Cetylpyridinium Chloride alone and 0.075% Cetylpyridinium Chloride associated with 0.28% zinc lactate in reduction of the viral load of SARS-CoV-2 in the oral cavity. Patients of both sexes, in the age-range between 18 and 90 years, diagnosed positive for SARS-CoV-2 by the RT-PCR method, and who demand oral hygiene care and other preventive and therapeutic dental procedures, will be included in this randomized clinical study.The study will comprise patients hospitalized in common beds, without mechanical ventilation - who will be divided into three groups. Some of these protocols with the use of antimicrobial solutions are hoped to be efficient in reducing the viral load in the oral cavity. This is a factor that could contribute to reducing contamination of the environment caused by aerosols resulting from dental procedures, in addition to helping with the improvement in biosafety protocols against SARS-CoV-2.

Full description

Each group of patients will receive specific interventions, as follows: 0.075% Cetylpyridinium Chloride mouthwash (Group 1); 0.075% Cetylpyridinium Chloride associated with 0.28% zinc lactate mouthwash (Group 2), negative control, distilled water (Group 3). To monitor the viral load, the following procedures will be performed: saliva collection, in time intervals before mouth rinsing with the solutions at baseline (T0), immediately after (T1), 30 min (T2), and 1 hour after mouth rinses (T3). SARS-CoV-2 will be quantified by Real Time quantitative reverse transcription polymerase chain reaction (RT-qPCR) assays.

Enrollment: 105 patients

Sex: All

Ages: 18 to 90 years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• positive for SARS-CoV-2 by the RT-PCR method,
• in common bed for minimum of 1 day and maximum of 5 days,
• ensuring that patients are no more than 10 days since showing the first symptoms,
• who are positive for SARS-CoV-2 in the first collection of oral fluid and saliva, and
• who demands oral hygiene care and other preventive and therapeutic dental procedures.

Exclusion criteria

• pediatric patients, t
• hose who tested negative for SARS-CoV-2 by the RT-PCR method at the time of recruitment or at the time of first oral fluid and saliva collection;
• those who exhibit oral ulcerations and other erosive lesions in the oral mucosa, which contraindicate the use of cetylpyridinium;
• patients who have bleeding in the oral cavity which prevents sample collections; patients who report history of allergy, irritations or other side effects derived from the use of these substances;
• patients who do not adhere to oral care protocols or those in whom it was not possible to perform these procedures.

Trial design

Primary purpose: Supportive Care

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Triple Blind

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105 participants in 3 patient groups, including a placebo group

CPC+Zn

Active Comparator group

Description:

patients submitted to mouth rinse with 0.075% Cetylpyridinium Chloride associated with 0.28% zinc lactate solution.

Treatment:

Other: CPC+ZN

CPC

Active Comparator group

Description:

patients submitted to mouth rinse with 0.075% Cetylpyridinium Chloride solution.

Treatment:

Other: CPC

Negative Control

Placebo Comparator group

Description:

patients submitted to mouth rinse with distilled water.

Treatment:

Other: Negative Control