Systemic Lupus Erythematosus
Conditions
Interventions
Group 2:Langchuangjing granule + Prednisone acetate tablets, hydroxychloroquine and other Western medicines for 12 weeks.
Group 1:Prednisone acetate tablets, hydroxychloroquine and other Western medicines for 12 weeks.
Sponsors
Nanjing University of Chinese Medicine Affiliated Hospital
Eligibility
Sex/Gender
All
Inclusion criteria
Inclusion criteria: 1.Meet the diagnostic criteria of SLE and the syndrome differentiation standard of TCM kidney deficiency and phlegm syndrome. 2.The age is between 18 and 65 years old, regardless of gender. 3.Patients who have used or are using hormone therapy. 4.Informed consent, volunteering to be tested. The process of obtaining informed consent should be in accordance with GCP regulations.
Exclusion criteria
Exclusion criteria: 1.Patients have combined with serious diseases such as infections and tumors. 2.There are other rheumatisms such as rheumatoid arthritis, scleroderma, polymyositis, and Sjogren's syndrome. 3.The condition is critical and it is difficult to make a definitive assessment of the effectiveness of this trial. 4.Pregnant, lactating women. 5.Persons with adequate informed consent cannot be given due to intellectual or behavioral disorders. 6.Suspected or indeed have a history of alcohol and drug abuse. 7.According to the judgment of the investigator, other lesions that have the possibility of reducing the enrollment or complicating the enrollment, such as frequent changes in the working environment, are likely to cause loss of follow-up. 8.Allergies, such as those who have a history of allergies to two or more drugs or foods; or those who are known to be allergic to the ingredients. 9.Patients who are participating in other drug clinical trials.
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| temperature;Blood Pressure;SLEDAI;blood sugar;metabolomics;proteomics; | — |
Countries
China
Contacts
Public ContactGuo Feng
Jiangsu Province Hospital of TCM
Outcome results
None listed