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A randomized controlled trial of Bi min fang granules and traditional Chinese medicine decoction in the treatment of persistent allergic rhinitis

Not Applicable
Conditions
allergic rhinitis(AR)
Registration Number
ITMCTR2200006157
Lead Sponsor
Guangdong Provincial Hospital of Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

? Subjects who meet the Chinese and Western diagnostic criteria for AR, those with Chinese medicine syndrome differentiation of Lung and Sleen deficiency, and those who meet the criteria for persistent allergic rhinitis (symptom onset = 4 days/week, and = 4 consecutive weeks).
? 18-65 years old, no gender limited.
? Subjects need informed consent, voluntarily accept the treatment according to the research allocation plan, basically can adhere to the treatment and follow-up plan, and have good compliance.
? Subjects are able to complete relevant records such as case report form as required.

Exclusion Criteria

? Patients who do not accept the contents of this trial.
? Patients combined with severe cardiovascular and cerebrovascular diseases, immunodeficiency, mental disorders or abnormal liver and kidney function and malignant tumors.
? For women who are pregnant or breastfeeding, if pregnancy is found during the trentment period, the test will be suspended.
? Patients who are easily lost to follow-up due to frequent changes in the work environment.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
total nasal symptom score, TNSS;
Secondary Outcome Measures
NameTimeMethod
the standardize dversion of the Rhinoconjunctivitis Quality of Life Questionnaire,RQLQ(S);eye symptom score;Rhinitis Control Assessment Test,RCAT;Use of anti-allergy medication scores;
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