Efficacy of ADW S-100 Ionized Water Nasal Spray in Decreasing SARS-Cov-2 Viral Load.
NCT ID: NCT05290987
Last Updated: 2022-11-17
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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TERMINATED
NA
13 participants
INTERVENTIONAL
2022-01-14
2022-11-08
Brief Summary
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The aim of this study is to evaluate whether the use of ADW S-100 ionized water nasal spray reduces the salivary and nasopharyngeal viral load during an 8-day follow-up of persons recently infected with SARS-Cov-2, and thus potentially decreases the risk of contamination of the entourage.
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Detailed Description
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Conditions
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Study Design
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RANDOMIZED
PARALLEL
PREVENTION
DOUBLE
Study Groups
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Advanced Water S-100 ionized nasal spray
2 sprays in each nostril, 6 times a day during 8 days
nasal spray
2 sprays in each nostril, 6 times a day
Nasal spray with purified water
2 sprays in each nostril, 6 times a day during 8 days
nasal spray
2 sprays in each nostril, 6 times a day
Interventions
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nasal spray
2 sprays in each nostril, 6 times a day
Eligibility Criteria
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Inclusion Criteria
2. Informed consent
3. Beneficiaries of a social security plan
4. Vaccinated or unvaccinated against SARS-COV-2:
* Vaccinated individuals have had a 3rd dose for at least one month, or have been infected with SARS-Cov-2 and have had 2 doses of vaccine for at least one month
* Unvaccinated persons are naïve to previous SARS Cov 2 infection
5. Positive nasopharyngeal RT-PCR test for selection with a Ct viral load ≤ 23
6. Have a phone and internet connection to access the entry application
Exclusion Criteria
2. Known hypersensitivity or allergy to any component of the test product.
3. Contraindication to nasal spray
4. Insufficient vaccination: any incomplete vaccination schedule
* either a 3rd dose within the last month
* or SARS-Cov-2 infection with less than 2 vaccine doses or with 2 vaccine doses less than 1 month old.
5. Any condition, including COVID, that is likely to result in hospitalization during study participation.
6. Conditions that may result in hospitalization during study participation.
7. Known pregnancy or positive urine pregnancy test at D0 by the nurse, or current breastfeeding
8. Participation in an antiviral clinical trial or other trial using a medical device for disease prevention COVID 19
18 Years
ALL
No
Sponsors
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MediAxe CRO
UNKNOWN
P & B Group
INDUSTRY
Responsible Party
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Principal Investigators
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Christophe Bouvier, Dr
Role: PRINCIPAL_INVESTIGATOR
independent oto rhino laryngologist
Locations
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Dr Bouvier's Office
Aix-en-Provence, , France
Countries
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Other Identifiers
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2021-A01861-40
Identifier Type: -
Identifier Source: org_study_id
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