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A multicenter, randomized, double-blind, placebo-controlled clinical study to evaluate the efficacy and safety of Yiqi Jiemin Decoction in the treatment of moderate to severe allergic rhinitis (lu

Phase 1
Recruiting
Conditions
allergic rhinitis
Registration Number
ITMCTR2200006831
Lead Sponsor
Dongzhimen Hospital of Beijing University of Traditional Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Recruiting
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

a. Age = 18, = 65;

b. Clinical symptoms: two or more of the symptoms, such as itching, sneezing, water like nasal discharge, and nasal congestion, occur in the nose, and the symptoms persist or accumulate for more than 1 hour every day, even accompanied by eye itching, tears, conjunctival congestion and other eye symptoms;

c. The severity of symptoms is assessed as moderate or severe, that is, the symptoms are severe or severe, which has a significant impact on the quality of life. The onset of symptoms is greater than 4d/week, and = 4 consecutive weeks

d. Skin prick test and serum specific IgE positive are at least consistent with one of the two indicators

e. Obtain the informed consent of the patient and be willing to participate in the experiment;

f. The liver and kidney function of the patient is normal, so as to avoid the error caused by abnormal liver and kidney function damage after taking traditional Chinese medicine;

g. The patient has a good mental status, and can objectively and accurately express their own symptoms and treatment effects.

Exclusion Criteria

a. The patient is in the acute attack period of asthma and cardiovascular and cerebrovascular diseases, or suffers from immunodeficiency disease, head and face trauma, tumor, or organ transplantation;

b. Women in pregnancy or lactation;

c. Patients who are using glucocorticoid (including oral and local external use) for more than one week;

d. Those who receive other clinical trials within 30 days.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
asal Symptom Rating Scale;
Secondary Outcome Measures
NameTimeMethod
Visual analog scale;Nasal endoscopic nasal sign score;Rhinoconjunctivitis Daily Quality of Life Questionnaire;
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