Carrageenan Nasal Spray for COVID-19 Prophylaxis

Objectives:

The primary objective is to determine whether carrageenan nasal and throat sprays reduce the risk of COVID-19 infection.

The secondary objectives are:

• To determine whether carrageenan nasal and throat spray reduces the severity and/or duration of COVID-19 infection;
• To determine whether carrageenan nasal and throat spray reduces the risk of infection with other respiratory viruses
• To determine whether carrageenan nasal and throat spray reduces the severity and/or duration of infection with other respiratory viruses
• To determine the usability of carrageenan nasal and throat spray for long term prophylaxis against respiratory viruses
• To determine the effect on of using the spray on quality adjusted life years and cost effectiveness

Study Design:

The study design consists of a double blind, randomised placebo-controlled trial. Of the 480 healthcare professionals recruited, 240 participants will be randomly allocated to each of either the treatment arm (verum Coldamaris plus i.e. Iota-carrageenan 0.12% plus 0.04% Kappa-Carrageenan in 0.5% saline) or placebo (Coldamaris sine i.e. 0.5% saline) arms. Participants will use the spray prophylactically into each nostril and throat three times per day for 8 weeks, during which time the participants will be invited to complete a daily symptom tracker questionnaire. COVID-19 infection during the trial period will be confirmed using viral PCR swabs (if symptomatic), SARS-CoV-2 serology at 14 days following onset of symptoms as well as trial entry and exit serology to detect asymptomatic infection during the study period.

Allocation to each group, treatment or placebo administration and data analysis will be blinded to both participant and investigator. The primary outcome measure will be acquisition of COVID-19 infection as confirmed by positive PCR swab taken at the time of symptoms or positive serology measured 2 weeks after symptom onset or seroconversion at the end of the trial (via trial entry and exit serology) to detect asymptomatic infection during the study period. Secondary outcome measured will include symptom types, severity and duration (recorded by the daily symptom tracker questionnaire), hospital admission and length of stay, oxygen saturation and radiological lung changes on admission, need for ventilatory support (oxygen therapy, CPAP, intubation & ventilation), haematological changes, intensive care admission and length of stay, mortality, subsequent familial/household COVID-19 infection and acquisition of non-COVID-19 upper respiratory tract infections.

Deliverables:

• This trial will help us to determine whether carrageenan nasal sprays significantly affect the primary outcome measure of acquisition of COVID-19 infection as confirmed by positive PCR swab taken at the time of symptoms or positive serology measured 2 weeks after symptom onset or at the end of the study.
• It will also determine the effect of carrageenan nasal sprays on secondary outcome measures which include types, severity and duration of symptoms, hospital admission and length of stay, need for ventilatory support and intensive care admission, mortality as well as familial or household COVID-19 infection and acquisition of other respiratory tract infections.
• We will also investigate whether haematological changes (FBC, CRP, U&E, Ferritin, LFT, LDH, Clotting, D-dimer, FDP, Vitamin D level) and demographic questionnaire findings can offer a predictive value for acquiring COVID-19 infection or determining severity and/or duration of resultant infection.
• To determine any associations between symptom severity and/or duration and prognosis in those with COVID-19.
• Determine usability and acceptability of nasal and throat spray as prophylaxis and affect on quality adjusted life years and cost effectiveness

Inclusion criteria

• Age ≥18 years;
• Study participants who have given informed consent, and received a copy of signed consent form prior to any study related procedures;
• Healthcare professionals (nurses, doctors, allied health professionals, health care assistants, operating department practitioners) working in Swansea Bay University Health Board initially as well as any other volunteers >18 years who have not previously tested positive for COVID19 or been vaccinated.
• Subjects agree to refrain from taking over the counter products intended to prevent, intervene in, or treat colds/flu, starting at study entry and continuing through week 10 of the study.

Exclusion criteria

Capacity, consent and conflicts of interest:

• The person lacks capacity;
• The subject is related to any study personnel or has any other close ties or conflicts of interest with the research team or the study sponsor;
• The subject has received any investigational drug or participated in a clinical trial within 4 weeks of entry to this study.
• Unable to complete the daily symptom tracker
• Unable to communicate in English or Welsh

Comorbidities:

• Known hypersensitivity or allergy to any component of the test product;
• Severe cardiovascular, endocrinological, neurological, respiratory, gastrointestinal disease, immune deficiency, autoimmune disease or a history or any current disease that is considered by the investigator as a reason for exclusion;
• Severe nasal septal deviation, nasal polyps or other non-infectious condition that could cause nasal obstruction;
• A history of any nasal or sinus surgery in the past that in the opinion of the investigator may influence the symptoms or spray administration;
• An unrelated infection that in the opinion of the investigator may influence symptoms (gastrointestinal infection, other viral diseases such as measles, mumps);

COVID-19 Status:

• Participants with proven COVID-19 infection (previous positive serology and/or viral PCR swab)
• Participants that have already received their vaccination or already booked in for their vaccination

Medications:

• Recent treatment of common cold that in the opinion of the investigator may influence symptoms (see Table 2)
• Participants taking any of the medications outlined in Table 2 during the trial period will be excluded