So far, the study has enrolled 75 participants and study leaders would like to enroll at least 25 more participants, though more are welcomed. This is a ten-week trial for each participant. For three of those weeks, participants will use a mouthwash containing chlorhexidine gluconate four times a day, and nasal swabs containing povidone iodine two times a day. Participants will report any COVID-19 symptoms or diagnoses during that time and will also collect nasal samples using shallow nostril swabs to allow measurement of SARS-CoV-2 virus levels. The study will track COVID-19 diagnoses and viral measurements (how much virus is in the nose) in study participants. Researchers anticipate having results of the study later this summer.
Povidone iodine and chlorhexidine gluconate are antiseptic agents commonly used in health care settings to kill microorganisms that can cause infections, and are often applied to the skin, nose, or mouth before and after surgery to prevent infections. In lab settings, these antiseptics have proven effective in killing coronaviruses, including the virus that causes COVID-19.
If you are interested in participating, please visit the website for more information. To enroll in the study, please contact the research coordinators at shield@medicine.wisc.edu or call 608-262-6560.
Daniel Shirley, MD, MS, medical director of infection control at UnityPoint Health – Meriter is co-principal investigator with Dr. Safdar. Both are infectious disease physicians at the University of Wisconsin School of Medicine and Public Health.
Editor’s note: Recruitment is complete and the study team is no longer seeking volunteers.