Can a needle in the face tame allergy symptoms?
NCT ID NCT07784491
First seen Aug 25, 2026 · Last updated Aug 28, 2026 · Updated 2 times
Summary
This trial asks whether adding a specific type of acupuncture—targeting a nerve bundle behind the nose—to a standard nasal steroid spray can ease allergic rhinitis symptoms like sneezing, congestion, and itching better than the spray alone. Adults with moderate-to-severe perennial allergic rhinitis will be randomly assigned to use the spray for four weeks, with or without twice-weekly acupuncture sessions. Researchers will compare changes in nasal symptoms, quality of life, and safety between the two groups, and check whether any benefits last after treatment ends.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Sphenopalatine ganglion acupuncture plus mometasone furoate nasal spray
- What this could lead to
- If adding this targeted acupuncture to a standard nasal spray improves symptom relief, it could offer a drug-free add-on option for people with allergic rhinitis.
- What could go wrong
- This is a single-center trial with a modest sample size, and results may not apply broadly. Acupuncture carries minor risks like soreness or bleeding, and the added benefit over the spray alone is not yet proven.
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Study facts
What this study's own registry entry says, in plain language.
- Phase
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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
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About 150 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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Aug 2026
An estimate. Start dates often move.
- Expected to finish
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Jan 2027
An estimate. End dates often move.
- 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.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- 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.
Show the full entry requirements Hide 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: * Diagnosis of allergic rhinitis according to the Chinese Guidelines for Diagnosis and Treatment of Allergic Rhinitis (2022 Revision), meeting all of the following criteria: * At least two of the following symptoms: paroxysmal sneezing, watery rhinorrhea, nasal itching, and nasal obstruction, with symptoms lasting or accumulating for at least 1 hour per day; ocular symptoms such as itching, tearing, or redness may also be present. * Anterior rhinoscopy or nasal endoscopy showing findings consistent with allergic rhinitis, such as pale or edematous nasal mucosa, turbinate swelling, and watery nasal secretions. * At least one positive allergen test, including a skin prick test, serum allergen-specific immunoglobulin E (sIgE) test, or nasal allergen provocation test. * No use of antihistamines, intranasal or systemic corticosteroids, leukotriene receptor antagonists, allergen immunotherapy, or other treatments that may affect efficacy assessment within 2 weeks before enrollment. * Baseline Total Nasal Symptom Score (TNSS) sufficient for efficacy assessment according to the study protocol. * Voluntary participation in the study and provision of written informed consent. * Exclusion Criteria: * Presence of acute upper respiratory tract infection, acute or chronic rhinosinusitis, nasal polyps, severe nasal septal deviation, rhinitis medicamentosa, vasomotor rhinitis, infectious rhinitis, or other forms of non-allergic rhinitis. * Presence of an autoimmune disease or a psychiatric or psychological disorder that may interfere with study participation or outcome assessment. * Pregnancy or breastfeeding. * Coagulation disorders, current use of anticoagulant medications, local skin infection at the acupuncture site, a tendency to develop excessive scarring, or inability to tolerate acupuncture. * Known severe hypersensitivity or contraindication to any component of the study medication or to the study intervention. * Current participation in another clinical study, or any other condition that, in the investigator's judgment, makes the participant unsuitable for this study.
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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
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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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
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Zhongshan Torch Development Zone People's Hospital
Zhongshan, Guangdong, China
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