Natural supplement astaxanthin tested as new asthma aid in dirty air

NCT ID NCT07507682

What the study statuses mean

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Recruitment status, easiest to join first

Recruiting now This study
This trial is taking on new participants right now.
Not yet recruiting
Registered, but not yet taking participants.
By invitation only
Not open to general applications. Only people the study team invites can take part.
Paused
Paused for now. It may or may not start again.
Ongoing
Running, but no longer taking on new participants.
Completed
The trial has finished. Results may not be published yet.
Stopped early
Stopped early, before it reached the end. That can be for many reasons, including safety.
Cancelled
Cancelled before anyone took part.

Expanded access (not trials)

Expanded access
Not a trial. This treatment can be requested outside a study, case by case, for people who qualify.
Expanded access (paused)
Not a trial. The treatment can normally be requested outside a study, but is unavailable right now.
Expanded access (ended)
Not a trial. The treatment could once be requested outside a study, but no longer can.
Approved
The treatment has been approved, so it is available normally rather than through this programme.

When the status isn't known

Details not published
The full record has not been published yet, so there is little to show here.
Status unknown
This status has not been confirmed recently, so it may be out of date.

First seen Jun 27, 2026 · Last updated Jun 27, 2026

Summary

This study tests whether astaxanthin, a natural antioxidant supplement, can improve lung function and reduce airway inflammation in adults with mild-to-moderate asthma. Participants will take astaxanthin and a placebo in random order for 4 weeks each, with a break in between. The study also measures air pollution exposure to see how it affects asthma symptoms and treatment response.

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

Not a phased trial

Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.

Participants

About 25 people

The number the study aims to enrol. It can still change while the study runs.

Expected to start

May 2026

An estimate. Start dates often move.

Expected to finish

Jul 2026

An estimate. End dates often move.

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

18 years and older

Sex

Anyone

Healthy volunteers

Accepted

You do not need to have the condition being studied to take part.

Show the full entry requirements

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+ y * Confirmed clinical diagnosis of mild-to-moderate asthma, defined as: * A physician diagnosed asthma condition consistent with BTS/NICE/SIGN (2024) * Asthma managed at GINA (2024) step 1-3 therapy level, with stable maintenance treatment for ≥4 weeks prior to enrolment * No asthma exacerbation requiring systemic corticosteroids within the preceding 6-8 weeks (those with suspected Asthma will be invited to a familiarisation and eligibility session where they will have clinical investigations to assess for asthma and thus be included or excluded) * Ability to demonstrate acceptable and repeatable spirometry in accordance with ATS/ERS standards * Willing to refrain from antioxidant and anti-inflammatory supplementation (e.g. Omega-3, turmeric, NSAID supplements) for the duration of the study * Not consuming high dietary ASTX sources (e.g., frequent salmonid or crustacean intake), assessed at screening * non-smoking and non-vaping * Able and willing to take daily study capsules and attend all required visits * Able and willing to complete home monitoring, including peak flow, air-quality monitoring, and questionnaires * Able to provide written informed consent Exclusion Criteria: * Current smokers or vapers which is associated with chronic airway remodelling, reduce hyperresponsiveness to bronchodilators, and increased neutrophilic inflammation, which can obscure the true effects of asthma-target interventions * Respiratory tract infection within the preceding 4 weeks * Pregnant or lactating individuals * Presence of significant co-morbidities, including CVD or autoimmune or systemic inflammatory diseases * Renal or gastrointestinal disorders that may affect astaxanthin absorption and metabolism * Known allergy or hypersensitivity to ASTX or any components of the study supplement * History of current evidence of alcohol or substance abuse * Participation in another interventional drug or supplement study within the preceding 3 months * Use of medicines with a narrow therapeutic index where supplement interactions may pose risk (e.g., ciclosporin/tacrolimus, warfarin), assessed by investigator * Other significant chronic respiratory disease (e.g., COPD, bronchiectasis)

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Conditions

The condition(s) this trial relates to.

asthma disease Respiratory Hypersensitivity

As listed by the trial registrant

The condition terms exactly as the trial's registrant entered them.

How to take part

Only the study team decides who joins. These are the ways to reach them.

  1. The places running it

    1 site. The list below names each one and where it is.

  2. The official record

    ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.

    Open the record ↗

  3. A doctor treating you

    A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.

Contacts and locations

Locations

  • Middlesex University

    RECRUITING

    London, Barnet, NW4 4BT, United Kingdom

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