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Inhibitory effect of needling sphenopalatine ganglion on the over activation of mucosal cells’ NF-kB signaling pathway in patients with allergic rhinitis

Inhibitory effect of needling sphenopalatine ganglion on the over activation of mucosal cells’ NF-kB signaling pathway in patients with allergic rhinitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2300073792
Enrollment
Unknown
Registered
2023-07-20
Start date
2023-10-01
Completion date
Unknown
Last updated
2023-07-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Allergic Rhinitis

Interventions

Treatment group :Needling Sphenopalatine Ganglion
Control group:puncturing Xiaguan acupoint

Sponsors

Beijing Tongren Hospital affiliated to Capital Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1: Clear diagnosis, with the age of 18-60 years old 2: Have a history of typical allergic rhinitis for more than 2 years and more than 10 years 3: Nasal secretion smear or peripheral blood IgE test is positive 4: The duration of the disease lasts for at least 6 weeks in each attack 5: Agree to follow the treatment plan, be able to understand and actively cooperate with the acupuncture treatment 6: Voluntary signing of the informed consent form.

Exclusion criteria

Exclusion criteria: 1: The following guan points are those with skin damage and infection within the 2cm radius of the center and are not suitable for acupuncture 2: Patients currently receiving allergen-specific immunotherapy 3: Treatment with ß receptor blockers (including systemic and topical medication) 4: Allergic rhinitis combined with moderate and severe asthma (FEV1 5: Patients who have received oral antihistamine drugs within the first 2 weeks of selection 6: Oral corticosteroids were used within the first 4 weeks of selection 7: Respiratory tract infection within the first 4 weeks of selection 8: Have participated in other clinical trials within 3 months 9: Patients with chronic sinusitis with / without nasal polyps, asthma and septum 10: Women with pregnancy period, lactation period and planned pregnancy 11: Patients with a history of immunosuppressive diseases (such as HIV infection), malignancy, autoimmune diseases, tuberculosis, cardiovascular insufficiency, or other serious organ systems as judged by the investigator 12: Other circumstances that the investigator considers is not suitable to participate in the trial.

Design outcomes

Primary

MeasureTime frame
Nasal resistance;Nasal resistance;Rhinitis (conjunctivitis) symptom score;The NF- ? B signaling pathway activation state;TNF-a?IgE?IL-10;lncRNA-mRNA;

Secondary

MeasureTime frame
Quality of Survival Questionnaire;

Countries

China

Contacts

Public ContactZhang Peng

Beijing Tongren Hospital affiliated to Capital Medical University

ellen0326@126.com+86 10 5826 3545

Outcome results

None listed

Source: ChiCTR (via WHO ICTRP) · Data processed: Feb 4, 2026