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Effect evaluation of Qidigushen prescription on idiopathic membranous nephropathy based on "real world"

Effect evaluation of Qidigushen prescription on idiopathic membranous nephropathy based on "real world"

Status
Recruiting
Phases
Phase 1
Study type
Observational
Source
ChiCTR
Registry ID
ChiCTR2300075449
Enrollment
Unknown
Registered
2023-09-05
Start date
2023-09-27
Completion date
Unknown
Last updated
2023-09-11

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

Conditions

Membranous nephropathy

Interventions

Western medicine section (Basic therapy combined with hormone and immunosuppressive agents):NA
Chinese and western medicine group (Western medicine group treatment on the basis of Qidi Gushen capsule):NA
Western medicine section (Primary therapy):NA
Chinese medicine section (Basic treatment combined Qidi Gushen capsule):NA

Sponsors

The First Affiliated Hospital of Shaanxi University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: 1.Those who meet the Western diagnostic criteria for primary membranous nephropathy (IMN); 2.Those who meet the diagnostic criteria of spleen, kidney, Qi and Yin deficiency syndrome of traditional Chinese medicine; 3.Age, gender is not limited; 4.Serum creatinine level is less than 265µmol/L; 5.24 hours urinary protein quantity is greater than or equal to 1g/d; 6.Voluntary signing of informed consent for clinical research.

Exclusion criteria

Exclusion criteria: 1.Confirmed by hepatitis B, systemic lupus erythematosus, tumor, diabetic nephropathy, drug damage and other factors secondary; 2.Patients with acute central nervous system disease, severe gastrointestinal disease, HIV infection history, psychiatric history; 3.Combined with serious diseases and dysfunction of other organs; 4.Patients with water and sodium retention, hyperkalemia, metabolic acidosis, and severe anemia that cannot be corrected by drugs are considered for renal replacement therapy; 5.Take other proprietary Chinese medicines related to this study, such as "Bailing capsule, Shenwu Yishen tablet, Yishenhuazhuo granules" and other proprietary Chinese medicines; 6.Pregnant or lactating women or investigators undergoing other clinical trials.

Design outcomes

Primary

MeasureTime frame
24h urinary protein quantification;Blood albumin;triglyceride;Total cholesterol;Antiphospholipase A2 receptor antibody titer;

Secondary

MeasureTime frame
Urea nitrogen;Serum creatinine;Uric acid;Glomerular filtration rate;

Countries

China

Contacts

Public ContactLi Xiaohui

The First Affiliated Hospital of Shaanxi University of Chinese Medicine

493472601@qq.com+86 138 9107 2931

Outcome results

None listed

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