NCT07459946Not yet recruiting
Research on Innovative Traditional Chinese Medicine Diagnosis and Treatment Technologies for Diabetic Nephropathy Driven by Multi-Omics and Artificial Intelligence
Research on New Diagnosis and Treatment Technologies for Major Traditional Chinese Medicine Advantage Diseases - Multi-Omics and Artificial Intelligence-Driven Innovative TCM Diagnosis and Treatment Technologies for Diabetic Nephropathy
Source: ClinicalTrials.gov · Last updated 10 Mar 2026
Brief summary (registry, in English)
With the help of the 'Traditional Chinese Medicine Specialty Alliance Platform-Multicenter RCT Clinical Research Database,' this platform can be used to conduct scientific research on various aspects of DKD, such as disease prediction, treatment effectiveness evaluation, and recurrence rate analysis, providing effective means to improve DKD remission rates, delay disease progression, and enhance patients' quality of life. By selecting the Jiade Yishen Xiaozheng Qufang formula and conducting multicenter, prospective, double-blind RCT studies, its clinical value in improving DKD remission rates can be verified. With the support of scientific research, DKD treatment strategies can be optimized, therapeutic efficacy improved, recurrence rates reduced, and disease progression delayed, thereby enhancing patients' quality of life.
- Status (registry)
- Not yet recruiting
- Study type
- Interventional
- Enrollment
- 198 (estimated)
- First submitted
- 4 Mar 2026
- Start date
- 12 Mar 2026
- Primary completion date
- 31 Dec 2026
- Lead sponsor
- Jiazhen Yin
- Diseases
- Chronic kidney disease
- NCT number
- NCT07459946
What you commit to
- Study type: Interventional
- Planned participants: 198
- From 12 Mar 2026 to the primary completion date, 31 Dec 2026
- No sites listed in no country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Currently taking Chinese herbal medicine or patent Chinese medicine with effects of tonifying deficiency, promoting blood circulation, or dispelling wind-dampness.
Other illness
- Acute kidney injury or renal function impairment caused by other reasons (recent rapid decline in renal function, or kidney damage caused by drugs, infections, etc.);
- Other primary or secondary kidney diseases (such as systemic lupus erythematosus, polycystic kidney disease, etc.);
- Uncontrolled severe complications (such as severe cardiovascular disease, uncontrolled hypertension, severe infections, etc.);
- Critical organ failure (severe diseases of the heart, liver, or lungs);
- Drug allergy or clear contraindications (allergic to the study drug or its components);
- Abnormal coagulation function, or undergoing anticoagulant therapy (such as warfarin, rivaroxaban, etc.) with bleeding risk;
Other
- Pregnancy or planned pregnancy (women currently pregnant or planning to become pregnant during the study);
- Non-cooperative or unable to follow the study protocol (unable or unwilling to comply with study requirements);
Who the study is looking for
- Meets the clinical diagnostic criteria for diabetic nephropathy;
- Aged 18-75 years, any gender;
- eGFR \>45 ml/min/1.73m²;
- 24-hour urine protein \<2.0 g/day;
- Exhibits Traditional Chinese Medicine patterns of deficiency, stasis, or rheumatic symptoms;
- Willing to participate in the study, able to attend regular follow-ups, and provide informed consent;
- Has maintained a stable basic treatment plan (including hypoglycemic, antihypertensive, and lipid-lowering therapies) for ≥1 month prior to enrollment; during the first 3 months after enrollment, ARB, finerenone, and SGLT2 inhibitor therapies should generally not be adjusted.
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
This page is information, not medical advice. Discuss any trial with your doctor.