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Research for 'Mind regulating acupuncture method' protocol in the treatment of allergic rhinitis

Research for 'Mind regulating acupuncture method' protocol in the treatment of allergic rhinitis

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR-TRC-11001245
Enrollment
Unknown
Registered
2011-04-03
Start date
2011-04-01
Completion date
Unknown
Last updated
2018-09-24

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

Conditions

allergic rhinitis

Interventions

Group A:Cetirizine 10mg P.O. once daily, for 4 consecutive weeks
Group B:Acupuncture: points selection: Yingxiang(LI20), Yintang, Baihui (GV20),Hegu(LI4), Feishu(BL13), Pishu(BL20),Shenshu(BL23),Ganshu(BL18), Dazhui(GV14),Taichong(LR3).Yingxiang(LI20),Yintang and B

Sponsors

Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: 1. Subject has experienced main symptoms (nasal congestion, rhinorrhea, sneezing and nasal itching)for more than 4 days a week and for more than 4 consecutive weeks; 2. Subject presenting moderate/severe condition meeting the diagnostic criteria; 3. Subject responding with positive skin test reaction to at least one inhaled allergen; 4. Subject shows a mean total nasal symptom score (TNSS)>=4 one week before acupuncture intervention; 5. Subject age ranges between 18 and 66 years old; 6. Subject is able to provide written informed consent.

Exclusion criteria

Exclusion criteria: 1. Patient has suffered from acute paranasal sinusitis or upper respiratory infection within the last 14 days; signs of chest inflammation showed in X-ray; 2. Patient with history of chronic paranasal sinusitis or chronic paranasal sinusitis showned by accessory nasal cavity X-ray examination; 3. Patient presenting organic nasal cavity disease or has undergone nasal cavity surgery; 4. Patient suffering from paroxysmal respiratory diseases such as asthma; 5. Patients taking H1 antihistamine, steroids, antihistamine, decongestant (nasal, oral or ophthalmic), corticosteroids, antibiotics, or prohibited medications listed in Appendix 1 within 14 days of enrollment; 6. Subject that received specific immunotherapy or systematic hormone therapy in the last year; 7. Subject that received acupuncture, moxibustion, cupping, nasal inhalation of herbal medicine, or other physical therapies in traditional medicine treatment within the last 14 days; 8. Subject that took herbal preparation for allergic rhinitis within the last 14 days; 9. Subject is pregnant, lactating or planning to become pregnant. 10. Subject suffering from tuberculosis, hepatitis, or with blood Cr, AST/ALT values twice higher than normal ranges; 11. Subject suffering from mental disorders; 12. Subject presenting with a smoking history of over 10 cigarettes daily, during 10 consecutive years; 13. Subject presenting scars on the needling location or suffering from systemic disease therefore being considered unsuitable for needling application; 14. Subject that has been estimated as unable to collaborate in the trial.

Design outcomes

Primary

MeasureTime frame
Total nasal symptom scores (TNSS);

Secondary

MeasureTime frame
Life Questionnaire (RQLQ);Total nonnasal symptom score (TNNSS);

Countries

China

Contacts

Public ContactJiping Zhao

Acupuncture Department, Dongzhimen Hospital Affiliated to Beijing University of Chinese Medicine

zjp7883@sina.com+86 13621382136

Outcome results

None listed

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