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Analysis of the Benefits and Characteristics of Patient Populations Benefiting from Tripterygium Glycosides Tablets in Idiopathic Membranous Nephropathy Patients Treated with Rituximab:A Single-Cente,Prospective,Randomized Controlled Study.

Analysis of the Benefits and Characteristics of Patient Populations Benefiting from Tripterygium Glycosides Tablets in Idiopathic Membranous Nephropathy Patients Treated with Rituximab:A Single-Center, Prospective, Randomized Controlled Study.

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025001687
Enrollment
Unknown
Registered
2025-09-09
Start date
2025-09-30
Completion date
Unknown
Last updated
2025-09-15

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

Conditions

Idiopathic Membranous Nephropathy

Interventions

The experimental group :The experimental group received Tripterygium Glycosides Tablets in addition to the baseline treatment given to the control group. The dosage was 2 tablets (10 mg/tablet) orally
Control group:they were treated with rituximab injection (RTX). RTX administration (100 mg/vial): Dosage:1 g per dose,administered intravenously.Frequency:Two doses in total,with a 2-week interval bet

Sponsors

The Affiliated Hospital of Jining Medical Univercity
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 80 Years

Inclusion criteria

Inclusion criteria: 1) Age = 18 years; 2) Diagnosis of IMN confirmed by renal biopsy, accompanied by typical nephrotic syndrome (NS) clinical manifestations; 3) Patients are informed about the study and provide signed informed consent.

Exclusion criteria

Exclusion criteria: 1) Secondary MN caused by autoimmune diseases (e.g.,systemic lupus erythematosus),drugs,viral hepatitis,malignancies,etc; 2) Patients with severe infections,psychiatric disorders,or neurological diseases; 3) Follow-up duration less than 12 months; 4) Patients allergic to the study medication; 5) Pregnant or lactating women.

Design outcomes

Primary

MeasureTime frame
24-hour urinary protein excretion;

Secondary

MeasureTime frame
peripheral blood CD19+ B cell levels;serum albumin;M-type phospholipase A2 receptor antibody(PLA2R antibody);serum creatinine;

Countries

China

Contacts

Public ContactXiaofen Ma

The Affiliated Hospital of Jining Medical Univercity

maxiaofenjyfy@126.com+86 156 6817 9566

Outcome results

None listed

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