Clinical Trials Directory

Trials / Completed

CompletedNCT04894409

Evaluation of Silver Nanoparticles for the Prevention of COVID-19

Evaluation of Silver Nanoparticles as an Oropharyngeal Product (Mouthwash) and Nasal Hygiene, by Health Personnel Working at the Tijuana General Hospital Exposed to Patients Diagnosed With Atypical Pneumonia Caused by SARS-CoV-2

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
231 (actual)
Sponsor
Cluster de Bioeconomia de Baja California, A.C · Academic / Other
Sex
All
Age
20 Years – 73 Years
Healthy volunteers
Accepted

Summary

In this research, silver nanoparticles (AgNPs) were tested in vitro and shown to have an inhibitory effect on SARS-CoV-2 infection in cultured cells. Subsequently, the investigators assessed the effects of mouthwash and nose rinse with ARGOVIT® silver nanoparticles (AgNPs), in the prevention of SARS-CoV-2 contagion in health workers consider as high-risk group of acquiring the infection in the General Tijuana Hospital, Mexico, a hospital for the exclusive recruitment of patients diagnosed with COVID-19.

Detailed description

SARS-CoV-2 infection in hospital areas is of a particular concern, since the close interaction between health care personnel and patients diagnosed with COVID-19, which allows virus to be easily spread between them and subsequently to their families and communities. Preventing SARS-CoV-2 infection among healthcare personnel is essential to reduce the frequency of infections and outbreaks during the pandemic. In a first step, silver nanoparticles (AgNPs) were tested in vitro to determine an inhibitory effect on SARS-CoV-2 infection in cultured cells. Subsequently, the investigators assess the effects of mouthwash and nose rinse with ARGOVIT® silver nanoparticles (AgNPs), in the prevention of SARS-CoV-2 contagion in health workers consider as high-risk group of acquiring the infection in the General Tijuana Hospital, Mexico, a hospital for the exclusive recruitment of patients diagnosed with COVID-19. The investigators present a prospective randomized study of 231 participants that was carried out for 9 weeks (during the declaration of a pandemic). The "experimental" group was instructed to do mouthwash and nose rinse with the AgNPs solution; the "control" group was instructed to do mouthwashes and nose rinse in a conventional way.

Conditions

Interventions

TypeNameDescription
DEVICEMouthwash and nose rinse with the AgNPs solutionThe "experimental" group was instructed to do mouthwash and nose rinse with the AgNPs solution for the prevention of SARS-CoV-2 infection in health workers
DEVICEMouthwashes and nose rinse in a conventional wayThe control group was instructed to do mouthwashes and nose rinse in a conventional way

Timeline

Start date
2020-04-24
Primary completion
2020-06-30
Completion
2020-09-29
First posted
2021-05-20
Last updated
2021-05-20

Locations

1 site across 1 country: Mexico

Source: ClinicalTrials.gov record NCT04894409. Inclusion in this directory is not an endorsement.