Could a common compound help fight COVID-19 and flu? small study explores
NCT ID NCT07254052
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This small pilot study tested whether a sustained-release ammonium chloride formula (with vitamin D) can reduce virus levels in adults with mild or moderate COVID-19 or influenza. 32 participants took either the active formula or a vitamin D-only control twice daily for 10 days. Researchers measured viral load changes and tracked symptoms, hospitalizations, and other outcomes to gather early evidence on this potential add-on treatment.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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32 people
The number who actually took part.
- Started
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Sep 2024
- Finished
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May 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult patients (≥18 years old) with mild or moderate COVID-19 or seasonal influenza infection were recruited at the Outpatients Clinic and the Emergency Department of Sotiria General Hospital for Chest Diseases in Athens, Greece and at "En Ygeia" outpatient clinic. Both inpatients and outpatients were eligible. All participants had a laboratory-confirmed diagnosis by rapid antigen testing and were enrolled within 3-5 days of symptom onset. Patients with severe disease, organ transplantation, pregnancy, or frailty score ≥5 were excluded. A total of 32 participants completed the study procedures.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Adults ≥ 18 years. * Positive rapid test for Sars-CoV-2 19 or influenza (performed at the Outpatients Clinic or the Emergency Department). * Informed consent. Exclusion Criteria: * Age \< 18 years. * Pregnancy, and/or lactation. * Denial of Informed Consent. * Known allergy to ammonium chloride or to any of the ACF, or VDF excipients. * Organ transplantation. * Frailty score ≥ 5.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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En Ygeia Clinic
Athens, 11524, Greece
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Sotiria General Hospital
Athens, Greece
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Other studies related to the condition(s) this trial covers.
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