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Clinical Efficacy and Mechanism Study of No. 1 Huyan Decoction in Treating Stage 3 Chronic Kidney Disease

Evaluation of Clinical Efficacy and Mechanism Study of No. 1 Huyan Decoction in Treating Stage 3 Chronic Kidney Disease

Status
Recruiting
Phases
Unknown
Study type
Observational
Source
ITMCTR
Registry ID
ITMCTR2025002283
Enrollment
Unknown
Registered
2025-11-21
Start date
2025-08-13
Completion date
Unknown
Last updated
2025-12-08

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

Conditions

Chronic kidney disease

Interventions

the observed population:with no intervention measures

Sponsors

The Affiliated Hospital of Nanjing University of Chinese Medicine (Jiangsu Provincial Hospital of Traditional Chinese Medicine)
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 65 Years

Inclusion criteria

Inclusion criteria: 1) Patients who meet the diagnostic criteria for Stage 3 Chronic Kidney Disease (CKD) and the TCM pattern differentiation criteria for chronic renal failure, specifically the pattern of kidney deficiency with dampness (heat) and blood stasis. 2) Aged between 18 and 65 years, irrespective of gender. 3) Provide informed consent and volunteer to participate in the trial. The process of obtaining informed consent must adhere to the principles of Good Clinical Practice (GCP).

Exclusion criteria

Exclusion criteria: (1) Patients with severe comorbidities of major organs, such as severe hepatic dysfunction (transaminase levels >3 times the upper limit of normal), malignant tumors, severe anemia (Hb <60 g/L), or a history of cardiovascular/cerebrovascular stent implantation within the past 3 months. (2) Patients with CKD secondary to autoimmune diseases, or those currently taking corticosteroids or immunosuppressants. (3) Patients with a known allergy to any component of the Chinese herbal medicine, or those with a history of severe allergic predisposition. (4) Pregnant or lactating women. (5) Patients judged by the investigator to have poor compliance or who are otherwise deemed unsuitable for trial participation.

Design outcomes

Primary

MeasureTime frame
estimated Glomerular Filtration Rate;

Secondary

MeasureTime frame
renal function;urinary albumin/creatinine ratio;complete blood count;blood lipids;iron metabolism;

Countries

China

Contacts

Public ContactWeiming HE

The Affiliated Hospital of Nanjing University of Chinese Medicine (Jiangsu Provincial Hospital of Traditional Chinese Medicine)

13851699906@163.com13851699906

Outcome results

None listed

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