Overview

The Efficacy of Pre-procedural Mouth Rinses on COVID-19 Saliva Viral Load

Status:
Recruiting
Trial end date:
2021-06-30
Target enrollment:
Participant gender:
Summary
Preoperative antiseptic mouth rinses have been widely used as a standard protocol before routine dental treatment reduces oral microorganism counts. During dental procedures, aerosolized microorganisms contaminate the dental environment and nearby surfaces and remain suspended for 4 hours. Thus, the reduction in the number of aerosolized microorganisms by pre-procedural rinsing may reduce cross-contamination between dentists, office personnel, and patients. Recent reviews have advocated the use of preoperative rinsing to control and reduce the risk of SARS-CoV-2 transmission. However, no clinical studies have been done yet to support the effectiveness of any pre-procedural oral rinses against SARS-CoV-2. The proposed study will mitigate the spread of COVID-19 disease in dental health care facilities and ensure the patients' good health and healthcare workers. The purpose of this clinical trial is to determine and compare the effectiveness of four commercially available, pre-procedural mouth rinses versus distilled water on viral load of SARS-CoV-2 found in the saliva of COVID-19 positive patients and to measure the pre-rinsing viral load with the post-rinsing at three-time points.
Phase:
Phase 4
Details
Lead Sponsor:
King Abdulaziz University
Treatments:
Cetylpyridinium
Eusol
Hydrogen Peroxide
Listerine
Povidone
Povidone-Iodine
Sodium Fluoride
Sodium Hypochlorite