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Clinical observation on the effect of Jingui Shenqi Wan Decoction in the treatment of allergic rhinitis with kidney Yang deficiency

Clinical observation on the effect of Jingui Shenqi Wan Decoction in the treatment of allergic rhinitis with kidney Yang deficiency

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2026001453
Enrollment
Unknown
Registered
2026-06-10
Start date
2026-07-01
Completion date
Unknown
Last updated
2026-06-22

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

Conditions

Allergic Rhinitis

Interventions

Experimental group:Jingui Shenqi Wan Decoction combined with Western medicine

Sponsors

Affiliated Hospital of Chengdu University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1. Meet the diagnostic criteria for allergic rhinitis (2022 Chinese guidelines); 2. Traditional Chinese medicine syndrome differentiation is kidney yang deficiency type, and the total symptom score is = 10 points; 3. Age 18-65 years old, gender is not limited; 4. Subjects must understand the purpose of the study, voluntarily participate, and sign informed consent.

Exclusion criteria

Exclusion criteria: 1. Pregnant and lactating women. 2. Those who have used antihistamines (such as loratadine, ebastine, etc.) within 1 week. 3. Those who use sodium perchromoglycate and leukotriene receptor antagonists within 2 weeks. 4. Those who have received biological agent treatment within 6 months. 5. Those who have received allergen-specific immunotherapy (desensitization therapy) within 5 years. 6. Those who have undergone major surgery within 4 weeks. 7. Those who have used systemic glucocorticoids (oral, intravenous, etc.) within 4 weeks. 8. Those who have alcohol abuse or abuse of illicit drugs currently or in the past 3 years. 9. Those who have recently used nasal glucocorticoids or nasal decongestants (within 2-4 weeks). 10. Those who have any active, acute or chronic nasal or pulmonary disease (including asthma) confirmed by medical history or physical examination. 11. Those who lack cooperation or understanding ability to complete the questionnaire.

Design outcomes

Primary

MeasureTime frame
Visual Analog Scale (VAS) for nasal symptoms;

Secondary

MeasureTime frame
Modified Rhinoconjunctivitis Quality of Life Questionnaire (mRQLQ);Traditional Chinese Medicine (TCM) Syndrome Score;Nasal Resistance;Acoustic Rhinometry;Nasal Patency Value (Peak Nasal Inspiratory Flow, PNIF);Overall Response Rate;Relapse Rate;

Countries

China

Contacts

Public ContactLi Xinrong

The Affiliated Hospital of Chengdu University of Traditional Chinese Medicin

amz.3@163.com+86 139 8176 7185

Outcome results

None listed

Source: ITMCTR (via WHO ICTRP) · Data processed: Jun 29, 2026