Skip to content

Evidence-based evaluation and efficacy mechanism of yishentongluoprescription in the treatment of diabetic kidney disease stage 3

A Randomized Controlled Double-blind Trial of yishentongluoprescription in the treatment of diabetic kidney disease stage 3

Status
Active, not recruiting
Phases
Unknown
Study type
Interventional
Source
ITMCTR
Registry ID
ITMCTR2000003601
Enrollment
Unknown
Registered
2020-08-21
Start date
2020-10-01
Completion date
Unknown
Last updated
2023-02-20

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

Conditions

diabetic kidney disease stage 3

Interventions

Sponsors

Henan University of Chinese Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: (1) Patients who are clinically diagnosed as DKD and meet the criteria of DKD Mogensen III liver and kidney yin deficiency and blood stasis syndrome established in this project, and kidney damage caused by non-DKD diseases is excluded; (2) Aged 18-75 years old; (3) Serum creatinine was relatively stable within 3 months before enrollment, and the change did not exceed 15%; (4) Reduce blood pressure by Western medicine, and introduce the end-of-period sitting resting diastolic blood pressure (DBP) <=90mmHg and the sitting resting systolic pressure (SBP) <=160mmHg; after basic hypoglycemic, the introduction of end-period glycosylated hemoglobin (HbA1c) is between 6-9%; (5) Accept treatment voluntarily and sign an informed consent form.

Exclusion criteria

Exclusion criteria: (1) Patients with type 1 diabetes; (2) Those who have acute complications of diabetes and urinary tract infection within 1 month; (3) Severe heart, brain, liver, and hematopoietic system and other serious diseases (cerebral infarction, cerebral hemorrhage, transient ischemic attack, myocardial infarction, unstable angina, heart failure, elevated transaminases) occurred in the 3 months before enrollment Up to 2 times the upper limit of the normal range) and those who have used glucocorticoids or immunosuppressants; (4) Those who have had active bleeding in 3 months; (5) Abnormal blood coagulation function; (6) Those with renal artery stenosis; (7) Pregnant or lactating women, or those who are preparing to become pregnant; (8) People with mental illness or cognitive impairment; (9) People with allergies or allergic to the components of the drug; (10) Participants in other clinical trials within 1 month before enrollment; (11) The investigator believes that others are not suitable to participate in this clinical trial.

Design outcomes

Primary

MeasureTime frame
urine albumin creatine ratio;urinary albumin excretion rates;

Secondary

MeasureTime frame
BUN;Quality of Life;Cys-c;CRP;serum creatinine concentration;TCM symptom score;fasting blood glucose;TNF-alpha;TC;UA;LDL-c;HbA1C;IL-6;eGFR;TG;HDL-c;IL-1;2hBG;

Countries

China

Contacts

Public ContactXu Jiangyan

Henan University of Chinese Medicine

xujiangyan2008@163.com+86 18236992803

Outcome results

None listed

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