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Evaluation of clinical efficacy of Modified Huangqi Chifeng Decoction in treating IgA Nephropathy proteinuia based on Chinese medicine pathogenesis of “deficiency-wind-stasis -toxin”

Evaluation of clinical efficacy of Modified Huangqi Chifeng Decoction in treating IgA Nephropathy proteinuia based on Chinese medicine pathogenesis of “deficiency-wind-stasis -toxin”

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR1900022100
Enrollment
Unknown
Registered
2019-03-25
Start date
2019-04-01
Completion date
Unknown
Last updated
2020-11-16

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

Conditions

IgA nephropathy

Interventions

Placebo Group:Placebo+telmisartan
Experimental group:Flavoured huangqi chifeng granules+telmisartan

Sponsors

Xiyuan Hospital, China Academy of Chinese Medical Sciences
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: ? The diagnosis was IgA nephropathy, and the pathologic reports of renal perforation were reported in all cases. ? No gender limitation, aged 18-70 years. ? Moderate proteinuria(24-hour urinary protein quantity is between 1.0-2.5g)accompanied or not accompanied by microscopic hematuria. ? CKD1-2(GFR=60ml/min/1.73m2). ? TCM syndrome differentiation accords with qi deficiency and blood stasis syndrome as well as wind pathogen and heat toxicity. ? Non-dialysis patients with infection, acidosis, electrolyte disturbance, hypertension and other aggravating factors are effectively controlled and the condition is stable. The BP is between 130-90/80-60mmHg. Potassium is in the normal range. ? Voluntarily accept this study and sign the informed consent form.

Exclusion criteria

Exclusion criteria: ? Secondary factors leading to proteinuria, such as purpura nephritis, lupus nephritis. ? Patients who have been treated by glucocorticoid, immunosuppressant, tripterygium wilfordii preparation in three months are not included. ? Having mental illness, infectious disease or pregnancy. ? Patients who have chronic liver disease, myocardial fibrosis or interstitial pulmonary fibrosis are not included. ? Patients with acute renal failure or after renal transplantation are not included. ? Participants who are participating in other interventional clinical trials.

Design outcomes

Primary

MeasureTime frame
Urine protein quantitation for 24 hours;Urine protein/creatinine;Routine urine;

Secondary

MeasureTime frame
TCM symptom score;Serum IgA/C3;Serum SIgA;Serum creatinine;

Countries

China

Contacts

Public ContactZhang Yu

Xiyuan Hospital, China Academy of Chinese Medical Sciences

zhangyu8225@126.com+86 13611079831

Outcome results

None listed

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