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临床试验/NCT07459946
NCT07459946尚未招募不适用

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

Jiazhen Yin0 个研究点目标入组 198 人开始时间: 2026年3月12日最近更新:
干预措施

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
198
主要终点
UACR/UAER/24-hour urinary protein returns to normal or decreases by 50% compared with before.

研究概览

简要总结

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.

详细描述

Cooperative units jointly carry out a prospective randomized placebo-controlled parallel double-blind study, relying on a multi-center clinical research platform, and verify through multi-center, prospective, double-blind RCT studies the clinical value of the Jia Jian Yi Shen Xiao Zheng Qu Feng Formula in improving the remission rate of DKD, in order to optimize the treatment strategy for DKD.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Treatment
盲法
Double (Participant, Investigator)

入排标准

年龄范围
18 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • 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.

排除标准

  • 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);
  • Pregnancy or planned pregnancy (women currently pregnant or planning to become pregnant during the study);
  • Drug allergy or clear contraindications (allergic to the study drug or its components);
  • Non-cooperative or unable to follow the study protocol (unable or unwilling to comply with study requirements);
  • Abnormal coagulation function, or undergoing anticoagulant therapy (such as warfarin, rivaroxaban, etc.) with bleeding risk;
  • Currently taking Chinese herbal medicine or patent Chinese medicine with effects of tonifying deficiency, promoting blood circulation, or dispelling wind-dampness.

研究组 & 干预措施

Experimental group

Experimental

Experimental group basic treatment+Jiajian Yishen Xiaozheng Qufeng Granules

干预措施: Jiajian Yishen Xiaozheng Qufeng Granules (Drug)

Control group

No Intervention

Basic treatment in the treatment group+simulated traditional Chinese medicine granules

结局指标

主要结局

UACR/UAER/24-hour urinary protein returns to normal or decreases by 50% compared with before.

时间窗: Western medical efficacy evaluation will be conducted at weeks 0, 4, 8, 12, 16, 20, and 24

次要结局

未报告次要终点

研究者

发起方
Jiazhen Yin
申办方类型
Other
责任方
Sponsor Investigator
主要研究者

Jiazhen Yin

Chief Traditional Chinese Medicine Physician

Hangzhou Hospital of Traditional Chinese Medicine

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