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Can a natural spray beat dust mite allergies? new study aims to find out

NCT ID NCT07196527

What the study statuses mean

This study's is highlighted.

Recruitment status, easiest to join first

Recruiting now
This trial is taking on new participants right now.
Not yet recruiting This study
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 Results may not be published yet.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This status has not been confirmed recently, so it may be out of date.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 26, 2026 · Last updated Jun 27, 2026 · Updated 1 time

Summary

This study tests whether a natural nasal spray (Puressentiel Allergy Protection) can reduce symptoms of dust mite allergies. Twenty adults with dust mite allergic rhinitis will receive either the spray or a saline placebo before a nasal allergen challenge. Researchers will measure symptom scores and nasal airflow to see if the spray offers relief.

What this could mean

Our plain-language read of the trial. This is informational only, not medical advice or a prediction.

Active substance
Puressentiel Allergy Protection Nasal Spray (SNPA)
What this could lead to
If it works, this could offer a natural, drug-free option to ease allergy symptoms like sneezing and congestion.
What could go wrong
This is a very small, early study with only 20 people. It may not show a clear benefit over plain saline spray.

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 20 people

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

Expected to start

Nov 2025

An estimate. Start dates often move.

Expected to finish

Feb 2027

An estimate. End dates often move.

Lead sponsor

A company

The lead sponsor is a pharmaceutical, biotech, or medical-device company.

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

Not accepted

This study is not open to healthy volunteers. The entry requirements below say who it is open to.

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:General inclusion criteria: * The patient must have given their express consent to participate in the study. * The patient must be affiliated with or a beneficiary of a health insurance plan. * The patient is at least 18 years of age. Inclusion criteria for the target population: * Patients who have already consulted the allergy department at Montpellier University Hospital. * Patients suffering from perennial rhinitis (or rhino-conjunctivitis) caused by dust mites, diagnosed more than one year ago. * In the case of asthmatic patients, asthma must be under control. * Patients who have been able to stop all treatment with antihistamines or nasal corticosteroids for one week prior to the start of the study (7 days and 1 month, respectively). * Patients covered by social security. Exclusion Criteria:5.4 Exclusion Criteria General exclusion criteria: * The patient is in a period of exclusion determined by a previous study. * The patient is under judicial protection, guardianship, or curatorship. * The patient is a minor. * The patient is not fluent in French. Exclusion criteria regarding interfering diseases or conditions: * The patient is pregnant and/or breastfeeding. * Patient sensitized to a perennial allergen in addition to dust mites. * Patient sensitized to a seasonal allergen, during the allergen's peak pollen season. * Patient who has had a viral infection within 4 weeks prior to the provocation test. * Patient treated or undergoing treatment with allergen immunotherapy. * Patient treated with antihistamines (7-day washout period) or nasal corticosteroids (1-month washout period). * Patients with severe uncontrolled asthma.

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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.

How to take part

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  1. The official record

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