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A Clinical Study on the Therapeutic Efficacy of Danggui Shaoyao San in Treating Diabetic Nephropathy and Its Impact on Coagulation Function Based on the HIF-1 Signaling Pathway

A Clinical Study on the Therapeutic Efficacy of Danggui Shaoyao San in Treating Diabetic Nephropathy and Its Impact on Coagulation Function Based on the HIF-1 Signaling Pathway

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2025002606
Enrollment
Unknown
Registered
2025-12-30
Start date
2025-11-01
Completion date
Unknown
Last updated
2026-01-12

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

Conditions

Type 2 diabetic nephropathy

Interventions

Control Group:Lifestyle and dietary interventions
control blood glucose, blood pressure, and blood lipid levels.
Treatment group:Administer Danggui Shaoyao San in addition to the control group (adjustable according to symptoms).

Sponsors

Hebei Medical University First Hospital
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 75 Years

Inclusion criteria

Inclusion criteria: (1) Age between 18 and 75 years (inclusive of 18 and 75 years); (2) Meet the diagnostic criteria and staging for the aforementioned type 2 diabetic nephropathy; (3) Meet the diagnostic criteria, staging, and pattern identification for the aforementioned traditional Chinese medicine diagnosis of xiaoke disease nephropathy.

Exclusion criteria

Exclusion criteria: Any of the following conditions apply: (1) kidney diseases caused by other reasons, such as hypertensive nephropathy, lupus nephritis, IgA nephropathy, etc.; (2) acute complications of diabetes in the past 3 months, such as diabetic ketoacidosis and hyperglycemic hyperosmolar coma, etc.; (3) severe cardiovascular, neurological, hematological, or psychiatric diseases; (4) pregnant, peripartum, or breastfeeding women; (5) participation in other clinical trials within 4 weeks prior to the start of treatment; (6) contraindications or allergies to this medication.

Design outcomes

Primary

MeasureTime frame
Serum Creatinine (SCr);Blood Urea Nitrogen (BUN);Estimated Glomerular Filtration Rate (eGFR);Fasting Blood Glucose (FBG);Glycated Hemoglobin (HbA1c);Hypoxia-Inducible Factor 1-alpha;

Secondary

MeasureTime frame
Urine Albumin-to-Creatinine Ratio (UACR);Urine Microalbumin (ALB);Total Cholesterol (TC);Triglyceride (TG);Low-Density Lipoprotein Cholesterol (LDL-C);High-Density Lipoprotein Cholesterol (HDL-C);8-hydroxydeoxyguanosine (8-OHdG);Malondialdehyde (MDA);Superoxide Dismutase (SOD);Plasma von Willebrand factor;Thrombomodulin;Plasminogen activator inhibitor-1;Fibrinogen;D-dimer (D-D);Thromboelastography Analysis;Traditional Chinese Medicine Syndrome Scoring;

Countries

China

Contacts

Public ContactDong Wen

Hebei Medical University First Hospital

1261911557@qq.com13102846329

Outcome results

None listed

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