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Clinical Efficacy and Mechanism Study of Compound Danshen Dripping Pills in Improving Diabetic Renal Fibrosis

Clinical Efficacy and Mechanism Study of Compound Danshen Dripping Pills in Improving Diabetic Renal Fibrosis

Status
Active, not recruiting
Phases
Phase 4
Study type
Interventional
Source
ChiCTR
Registry ID
ChiCTR2500107551
Enrollment
Unknown
Registered
2025-08-13
Start date
2025-09-01
Completion date
Unknown
Last updated
2025-08-18

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

Conditions

Diabetic nephropathy

Interventions

Intervention group:ake 10 pills of Compound Danshen Dripping Pills each time, 3 times a day.
Control group:Conventional treatment

Sponsors

General Hospital of Central Theater Command of the Chinese People's Liberation Army
Lead Sponsor

Eligibility

Sex/Gender
All
Age
18 Years to 60 Years

Inclusion criteria

Inclusion criteria: (1) Aged 18-60 years, regardless of gender; (2) Clearly diagnosed with DKD according to the diagnostic criteria for diabetic kidney disease in the 2021 Chinese Clinical Practice Guidelines for Diabetic Kidney Disease; eGFR > 45 ml·min?¹·(1.73m²)?¹, urinary albumin-to-creatinine ratio > 30mg/g (stages G1-3aA2-3); glycosylated hemoglobin (HbA1c) is 7.0%-10.0%. (3) The study protocol was reviewed and approved by the Ethics Committee, and all patients signed written informed consent forms before participation.

Exclusion criteria

Exclusion criteria: (1) Type 1 diabetes or other special types of diabetes; (2) Pregnant, lactating women, or women planning to become pregnant; (3) Those taking Compound Danshen Dripping Pills or other Chinese patent medicines and Chinese herbal medicines; (4) Patients with other kidney diseases, or autoimmune diseases (rheumatism, asthma, etc.); (5) Patients with acute diabetic complications; (6) Patients with severe digestive system diseases who cannot tolerate drug treatment; (7) Patients with tumors, severe lesions of important organs such as heart, liver and kidney, coagulation dysfunction, large-area cerebral infarction, or those with language disorders or consciousness disorders.

Design outcomes

Primary

MeasureTime frame
N-cadherin;E-cadherin;

Secondary

MeasureTime frame
ROCK;MYPT1;Scr;UACR;UTP;eGFR;NAG;RBP;a1-MG;ß2-MG;

Countries

China

Contacts

Public ContactDong Jing

General Hospital of Central Theater Command of the Chinese People's Liberation Army

364745333@qq.com+86 189 7140 5826

Outcome results

None listed

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