Xylitol Based Nasal Spray for COVID-19 Treatment
Respiratory Viral Infection

About this trial
This is an interventional treatment trial for Respiratory Viral Infection
Eligibility Criteria
Inclusion Criteria: Capable of understanding and providing signed informed consent and ability to adhere to the requirements and restrictions of this protocol; Adult aged ≥18 years old with at least two comorbidities: diabetes (type 1 &2), obesity (BMI >30), hypertension, chronic heart disease, chronic pulmonary disease, chronic liver disease. Internet access and capability and willingness to participate in audio or audio/video engagements with medical professionals, receive texts, emails, and phone calls from study staff and have a device and reasonable cellular data or other internet access to submit daily study required information using a smart phone, tablet, laptop, or desktop computer during the study period; COVID-19 infection confirmed with a laboratory SARS-CoV-2 RT-PCR nasal swab; Specimen collected within the past 48 hours; Mild COVID-19 symptoms which may include fever, cough, sore throat, malaise, headache, muscle pain, gastrointestinal symptoms, lack of taste or smell without shortness of breath Exclusion Criteria: Not fit to consent and unable to follow the protocol; Age <18 years; Current tracheostomy or laryngectomy; Hypersensitivity to the active substance or to any of the excipients; Concomitant respiratory therapy such as oxygen or ventilator support. Positive airway pressure for obstructive sleep apnea is permitted if treatment was established with good compliance at least 3 months before enrolment; Need for hospitalisation for any reason; Inability to safely self-administer nasal spray Any clinical contraindications, as judged by the Qualified Medical Practitioner; Clinical signs indicative of moderate, severe or critical COVID severity symptoms (as defined by FDA COVID-19 Guidance Document) Mentally or neurologically disabled patients who are considered not fit to consent to their participation in the study; Lactating, pregnant or planning to become pregnant during the study period; Diagnosed with prior COVID-19 infection (>48 hours from the time the test is reported prior to the time of screening). No relevant comorbidity or only one comorbidity
Sites / Locations
Arms of the Study
Arm 1
Arm 2
Experimental
Placebo Comparator
Interventional
Control
The participants will receive Xylitol based nasal spray
The participants will receive saline based placebo