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Clinical Trials in China / NCT07784491
Starting soon Not applicable

Sphenopalatine Ganglion Acupuncture for Allergic Rhinitis

NCT07784491 · tracked via the Priya Life Science China tracker
Sponsor
Zhongshan Torch Development Zone People's Hospital
Phase
Not applicable
Started
2026-08-31
Last updated
2026-08-28

Condition(s) studied

Allergic Rhinitis

Investigational drug(s) / intervention(s)

Sphenopalatine Ganglion AcupunctureMometasone furoate nasal spray

Sphenopalatine Ganglion Acupuncture: Sphenopalatine ganglion acupuncture will be performed twice weekly for 4 consecutive weeks, for a total of 8 treatment sessions. Acupuncture will be performed alternately on the left and right sides without needle retention.

Mometasone furoate nasal spray: Mometasone furoate nasal spray will be administered as two sprays into each nostril once daily for 4 consecutive weeks.

Study summary

Allergic rhinitis can cause sneezing, a runny or blocked nose, and nasal itching, which may affect daily activities and quality of life. Nasal corticosteroid sprays are commonly used to control these symptoms, but some people may still have bothersome symptoms.

The purpose of this study is to find out whether adding sphenopalatine ganglion acupuncture to mometasone furoate nasal spray can improve allergic rhinitis symptoms more than using the nasal spray alone, and to evaluate the safety of this treatment.

Adults with moderate-to-severe perennial allergic rhinitis will be randomly assigned to one of two treatment groups. Both groups will use mometasone furoate nasal spray for 4 weeks. Participants in one group will also receive sphenopalatine ganglion acupuncture twice a week for 4 weeks. Researchers will compare changes in nasal symptoms, quality of life, use of rescue medication, clinical examination findings, and adverse events between the two groups. Participants will also be followed after treatment to assess whether the treatment effects are maintained.

Eligibility

Sex
ALL
Min age
Max age
Healthy volunteers
No
* 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.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Zhongshan Torch Development Zone People's Hospital Zhongshan Guangdong

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT07784491 on ClinicalTrials.gov ↗ ← All trials in China