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The prospective cohort study on differentiation and treatment of membranous nephropathy by Wenyang Huaji method

The prospective cohort study on differentiation and treatment of membranous nephropathy by Wenyang Huaji method

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
DRKS
Registry ID
DRKS00022948
Enrollment
296
Registered
2020-11-23
Start date
2020-11-10
Completion date
Unknown
Last updated
2025-04-07

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

Conditions

N05.2

Interventions

Group 1: Take Mahuang Fuzi Tang and Shenzhuo Tang without immunosuppressive therapy more than 6 months. Group 2: Not take Mahuang Fuzi Tang and Shenzhuo Tang more than 6 months.

Sponsors

Beijing Hospital of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ?Conforms to the MN diagnostic criteria. ?Conforms to the diagnostic criteria of Shaoyin Taiyin syndrome. ?The patient has signed the informed consent. ?Between the ages of 18 and 75. ?CKD stage I-III, eGFR>30ml/min, serum albumin >15g/L.

Exclusion criteria

Exclusion criteria: ?Progressive membranous nephropathy (progressive decrease of renal function;Kidney biopsy showed necrotizing capillaritis and > 50% large crescent), accompanied by IgA nephropathy, diabetic nephropathy and other kidney diseases. ?Confirmed hepatitis B, systemic lupus erythematosus, tumor, drug damage and other factors secondary and need to actively treat the primary disease, such as active hepatitis B and persistent liver function test transaminase abnormalities, or anti-nuclear antibodies, double Abnormal strand DNA, ANCA or other indicators of immune disease. ?With acute central nervous system disease, severe gastrointestinal disease, a history of HIV infection, a history of mental illness or a history of malignancy. ?With other organ diseases and dysfunction, and with life-threatening complications such as severely infected persons. ?Pregnant or lactating women. ?Other clinical trials are under study.

Design outcomes

Primary

MeasureTime frame
To evaluate the efficacy of Mahuang Fuzi Tang and Shenzhuo Tang in treating MN. Patients were followed up once every 28 days since enrollment, with no more than 5 days before and after the enrollment, and each case was followed up at least 18 times, or until the death of the patient or the occurrence of a decrease in the glomerular filtration rate to 50%, or the occurrence of cardiovascular and cerebrovascular events. At each follow-up, we collected the current symptoms of the patients, as well as 24-hour urinary protein quantification and serum albumin values, and compared them with the status before enrollment to see whether the patients were in remission or not.

Secondary

MeasureTime frame
To evaluate the safety of Mahuang Fuzi Tang and Shenzhuo Tang in treating MN. Patients were followed up once every 28 days since enrollment, with no more than 5 days before and after the enrollment, and each case was followed up at least 18 times, or until the death of the patient or the occurrence of a decrease in the glomerular filtration rate to 50%, or the occurrence of cardiovascular and cerebrovascular events. At each follow-up, we will collect the patients' liver function, renal function and electrolytes, and compare them with the status before enrollment, so as to understand whether the patients have liver and kidney function injury and other adverse reactions.

Countries

China

Contacts

Public ContactBaoli Liu

Beijing Hospital of Traditional Chinese Medicine

liubaoli@bjzhongyi.com+86 18901051212

Outcome results

None listed

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