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The efficacy and safety of Ganduqing granule for treating common cold with qi deficiency leading to lingering of evil syndrome: a randomized, double-blind, placebo, parallel-group, multicenter- controlled trial

Not Applicable
Not yet recruiting
Conditions
Common Cold
Registration Number
ITMCTR1900002681
Lead Sponsor
Hospital of of Chengdu University of Traditional Chinese Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Pending
Sex
All
Target Recruitment
Not specified
Inclusion Criteria

(1) Meet the diagnosis of common cold according to Western medicine;
(2) Meet the diagnosis of common cold with qi deficiency syndrome according to Traditional Chinese Medicine;
(3) Repeated colds every year, more than 4 times;
(4) Symptom presenting within 48 hours;
(5) Aged between 18 and 70 years;
(6) Voluntarily participate and provide signed informed consent.

Exclusion Criteria

(1) Influenza;
(2) Patient's body temperature over 39 degree C;
(3) White blood cell count > 12.0 x 10^9/L and/or neutrophil percentage > 80%;
(4) Patients with other infectious diseases of the respiratory tract, such as acute herpetic pharyngitis, acute viral pharyngitis, acute herpetic laryngitis, acute viral laryngitis, acute tonsillitis, and pneumonia;
(5) Liver function levels (alanine aminotransferase (ALT) and aspartate aminotransferase (AST)) 1.5 times higher than the upper limit of normal or abnormal serum creatinine;
(6) Allergic or possibility of being allergic to the ingredients in the study drug;
(7) Patients with severe cardio-cerebrovascular, lung, kidney or hematopoietic system diseases;
(8) Patients who have participated in other drug clinical trials within one month or are participating in other drug clinical trials;
(9) Other medicines (including cold, antibiotics, antivirals and similar traditional Chinese medicines) that have been used to treat the disease since symptom presenting within 48 hours;
(10) Pregnant and lactating women;
(11) Psychiatric patients;
(12) Identified by the investigator as inappropriate to participate in this study.

Study & Design

Study Type
Interventional study
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

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