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A randomized controlled study of Yiqi Yangyin Qufeng Formula in the treatment of early stage IgA nephropathy

Development of in-hospital preparation of traditional Chinese medicine based on phased treatment of IgA nephropathy

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025000277
Enrollment
Unknown
Registered
2025-02-16
Start date
2025-06-01
Completion date
Unknown
Last updated
2025-03-03

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

Conditions

IgA nephropathy

Interventions

treatment group:conventional treatment+ Yiqi Yangyin Qufeng formula

Sponsors

The Third Affiliated Hospital of Zhejiang Chinese Medical University
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Have been diagnosed with IgA nephropathy and meet the diagnostic criteria for CKD stage 1-2. (2) Have been diagnosed with the "Qi Yin Deficiency Syndrome" in TCM syndromes. (3) Adult subjects ages 18-75 years. (4) Have achieved good control of infections/electrolyte disorders/hypertension etc. (5) Have not participated in other clinical trials in the past six months and can comply with study procedures and follow-up.

Exclusion criteria

Exclusion criteria: (1) Patients who require immediate dialysis treatment and are currently receiving hormone nonsteroidal anti-inflammatory drug or immunosuppressive therapy; (2) Patients with severe arrhythmia acute heart failure myocardial infarction acute stroke unstable angina and NYHA grade IV;   (3) Patients with acute infectious diseases and surgical and traumatic stress;   (4) Merge patients with chronic infectious diseases such as active and delayed chronic hepatitis B decompensated liver cirrhosis or active tuberculosis; (5) Patients with severe organ dysfunction that affects survival such as malignant tumors HIV infection etc; (6) Patients with severe primary diseases such as cardiovascular hematological neurological digestive and respiratory systems and with a clear tendency towards bleeding; (7) Individuals with life-threatening complications such as hyperkalemia and heart failure; (8) The GFR fluctuation range within the first 3 months of enrollment is = 30%;   (9) Individuals with severe allergic constitution who are allergic or intolerant to certain drugs known in this study;   (10) Pregnant or lactating patients; (11) Individuals with a history of drug abuse or those who have been treated with immunosuppressants or glucocorticoids in the past 3 months; (12) Individuals with a history of major bleeding or blood transfusion in the past 3 months and signs of severe clinical infection or acidosis;   (13) Patients who are currently participating in other clinical trials or who are using other traditional Chinese medicine treatments at the same time that affect the efficacy assessment;   (14) Those who are preparing or have already undergone kidney transplantation and those with acute renal failure or chronic renal failure accompanied by acute exacerbation requiring immediate replacement therapy;   (15) Patients with acute kidney damage caused by post-renal factors such as obstruction (including stones urate crystals tumors etc.); (16) Patients with a history of mental illness or communication cognitive impairment who have poor compliance and are unable to cooperate;   (17)Non-yellow.

Design outcomes

Primary

MeasureTime frame
URBC;24h UPQ;

Secondary

MeasureTime frame
TCM syndrome score scale;frequency of infections;UACR;eGFR;

Countries

China

Contacts

Public ContactLu Keda

The Third Affiliated Hospital of Zhejiang Chinese Medical University

lukedaq@126.com13757175879

Outcome results

None listed

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