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Prospective randomized controlled study on the treatment of idiopathic podocytopathies by Yuebi Decoction combined with Fangji Huangqi Decoction

Prospective randomized controlled study on the treatment of idiopathic Podocytopathies by Yuebi Decoction combined with Fangji Huangqi Decoction

Status
Active, not recruiting
Phases
Early Phase 1
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2400087035
Enrollment
Unknown
Registered
2024-07-17
Start date
2024-08-01
Completion date
Unknown
Last updated
2024-07-22

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

Conditions

idiopathic podocytopathies

Interventions

Control group:Valsartan capsule, 80mg once daily for 48 weeks
Daglizin tablet, 10mg once daily for 48 weeks.
Experimental group:Valsartan capsule, 80mg once daily for 48 weeks
Daglizin tablet, 10mg once daily for 48 weeks
Yuebi Decoction and Fangji Huangqi decoction, twice a day, one pack each time, a total of 48 weeks.

Sponsors

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 70 Years

Inclusion criteria

Inclusion criteria: 1. The pathologic types of renal puncture and biopsy are primary minimal change disease (MCD), primary focal segmental glomerulosclerosis (FSGS) and primary membranous nephropathy (MN). 2. The clinical manifestation is proteinuria, which may be combined with hematuria, edema, hypertension and renal insufficiency. 3. When enrolled, the glomerular filtration rate was >30ml/min·1.73m2 (calculated according to EPI formula). 4. 24-hour urinary protein quantity =1.0g and <3.5g at the time of enrollment. 5. Age =18 years old and =70 years old, regardless of gender. 6. Patients who have signed informed consent.

Exclusion criteria

Exclusion criteria: 1. Patients with chronic kidney disease stage 4, stage 5 and kidney replacement therapy. 2. Patients with contraindications to valsartan capsules or daglipzin tablets, including renal artery stenosis, hyperkalemia, isolated kidney, urinary tract infection, etc. 3. Patients with severe infection, malnutrition, and acute renal failure. 4. Serious damage to heart, liver or brain function or other serious underlying diseases. 5. People who are known to be allergic to the Chinese medicine ingredients used. 6. Pregnant or lactating women. 7. People with severe mental illness. 8. Have participated in or are undergoing other clinical trials within 1 month before enrollment.

Design outcomes

Secondary

MeasureTime frame
Blood lipid;TCM syndrome score;Urine podocyte damage marker protein;

Primary

MeasureTime frame
Routine urine test;24-hour urinary protein quantity;Serum albumin;Renal function;Glomerular filtration rate;

Countries

China

Contacts

Public ContactTianwen Yao

Yueyang Hospital of Integrated Traditional Chinese and Western Medicine, Shanghai University of Traditional Chinese Medicine

yaotianwendc@126.com+86 159 0181 9930

Outcome results

None listed

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