Nasal sponge steroid shows promise for long COVID smell loss
NCT ID NCT05970731
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested whether a steroid (beclomethasone) placed directly in the nose using a tiny sponge could help people who lost their sense of smell after COVID-19. Sixteen adults with smell loss lasting over 3 months received either the steroid or a placebo sponge twice, two weeks apart. The main goal was to see if the treatment led to a meaningful improvement on a smell test.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- beclomethasone (a steroid) delivered via a nasal sponge
- What this could lead to
- If it works, this could point toward a treatment for smell loss after COVID-19.
- What could go wrong
- This is a very small early-phase trial with only 16 people, so results may not apply widely. The treatment is also short-term and may not restore smell for everyone.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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16 people
The number who actually took part.
- Started
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Sep 2023
- Finished
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Oct 2024
- Lead sponsor
-
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.
- 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: * Post-COVID hyposmia lasting greater than 3 months following COVID19 by history * Male or female, aged 18 years or older Exclusion Criteria: * Pregnancy or lactation * Known allergic reactions to components of microsponge (including shellfish) or to beclomethasone * Known diagnosis of glaucoma * Febrile illness within 1 week * Treatment with another investigational drug or other intervention within 3 months * Active sinonasal disease by nasal exam, i.e. rhinosinusitis, nasal polyps * Adults unable to consent * Prisoners, employees or subordinates * Individuals who are not yet adults (infants, children, teenagers)
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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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Duke University Medical Center
Durham, North Carolina, 27710, United States