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Clinical efficacy and safety observation of Xinyi San modified granules in the treatment of allergic rhinitis with deficient cold of lung Qi syndrome

Clinical efficacy and safety observation of Xinyi San modified granules in the treatment of allergic rhinitis with deficient cold of lung Qi syndrome

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400083496
Enrollment
Unknown
Registered
2024-04-26
Start date
2024-04-30
Completion date
Unknown
Last updated
2024-04-29

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

Conditions

allergic rhinitis

Interventions

Granule group:Xinyi San modified granules++Basic western medicine treatment
decoction group:Xinyi San modified decoction+Basic western medicine treatment
blank control group:For basic treatment of western medicine, Fluticasone Propionate Nasal Spray (produced by Fushuna, GlaxoSmith K line S. A, specification 50ug/120 spray, once a day, nasal spray 2 ti

Sponsors

Longhua Hospital Affiliated to Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1: Patients who meet the diagnostic criteria and traditional Chinese medicine syndrome criteria; 2: No western medicine, Chinese medicine, acupuncture and moxibustion and other treatments for allergic rhinitis within 2 weeks before enrollment; 3: Between the ages of 18 and 70; 4: Having cognitive ability, able to correctly read and understand informed consent forms, as well as independently fill out relevant scales for this study, voluntarily participate in this project.

Exclusion criteria

Exclusion criteria: 1:Patients who do not meet the diagnostic criteria; 2:Patients under the age of 18 or over 70 years old; 3:Patients with nasal complications and other organic diseases related to the nasal cavity; 4:Individuals with accompanying mental illness or other serious diseases of the internal and external medical systems; 5: Pregnant and lactating women; 6:Patients who are allergic to the investigational drug; 7:Individuals who have used other relevant treatment methods within 2 weeks; 8:Individuals who cannot understand the content of the scale and are unable to cooperate with examinations, treatments, and follow-up.

Design outcomes

Primary

MeasureTime frame
Nose and eye symptom score;

Secondary

MeasureTime frame
TCM Syndrome;EOS;IgE;Inflammatory cytokines;

Countries

China

Contacts

Public ContactHong Fang

Shanghai University of Traditional Chinese Medicine Affiliated Longhua Hospital

15000297742@163.com+86 150 0029 7742

Outcome results

None listed

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