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Naoxintong Capsule for Diabetic Nephropathy With Dampness Retention Pattern: A Multicenter, Randomized, Double-Blind, Placebo-Controlled TrialAcronymNXT-DKD (NXT-DKD)

2026年7月8日 更新者：Chen Xiangmei

Evidence-Based Evaluation of Naoxintong Capsule in the Treatment of Diabetic Nephropathy With Dampness Retention Pattern: A Multicenter, Randomized, Double-Blind, Placebo-Controlled Clinical Trial

Diabetic nephropathy (DN) is a leading cause of end-stage kidney disease worldwide and is associated with a high risk of cardiovascular events and mortality. Despite current standard therapies including renin-angiotensin system inhibitors (ACEI/ARB), glycemic control, and blood pressure management, disease progression remains inadequately controlled in many patients.

Naoxintong Capsule is a traditional Chinese medicine formulation composed of 16 herbal ingredients (Astragalus membranaceus, Prunus persica seed, Carthamus tinctorius, Paeonia lactiflora, Angelica sinensis, Ligusticum chuanxiong, Boswellia carterii, Commiphora myrrha, Salvia miltiorrhiza, Achyranthes bidentata, Cinnamomum cassia, Morus alba, Spatholobus suberectus, Buthus martensii, Pheretima aspergillum, and Hirudo nipponica). It has been widely used in China for cardiovascular and cerebrovascular diseases, with demonstrated effects on endothelial protection, anti-inflammation, anti-thrombosis, and plaque stabilization.

This multicenter, randomized, double-blind, placebo-controlled trial aims to evaluate the efficacy and safety of Naoxintong Capsule added to standard conventional therapy in slowing the progression of diabetic nephropathy and providing cardiovascular protection. A total of 410 patients with Type 2 diabetic nephropathy will be randomized (1:1) to receive either Naoxintong Capsules (4 capsules, 3 times daily) or matching placebo, in addition to standard therapy, for 12 months. The primary outcome is the annual rate of decline in estimated glomerular filtration rate (eGFR). Secondary outcomes include changes in proteinuria, CKD stage progression, time to end-stage kidney disease, major adverse cardiovascular events, TCM syndrome scores, and quality of life measures.

研究概览

地位

尚未招聘

条件

干预/治疗

详细说明

BACKGROUND AND RATIONALE

Diabetic nephropathy (DN) is the leading cause of chronic kidney disease (CKD) and end-stage kidney disease (ESKD) in economically developed countries. China has the largest diabetic population globally, and DN now accounts for approximately 30% of new dialysis patients. Despite the beneficial effects of ACE inhibitors (ACEI) and Angiotensin II receptor blockers (ARB) in the microalbuminuric stage, landmark trials (RENNAL, IDNT, VA NEPHRON-D) have shown that these agents alone or in combination fail to significantly reduce cardiovascular events and all-cause mortality in advanced DN. There is an urgent need for novel therapeutic approaches to slow DN progression and improve survival.

Naoxintong Capsule (National Drug Approval No.: Guoyaozhunzi Z20025001) is a well-established traditional Chinese medicine formulation that has been widely used in China for cardiovascular and cerebrovascular diseases. It comprises 16 herbal and animal-derived ingredients that collectively exert effects through endothelial protection, anti-inflammatory activity, inhibition of thrombosis, and plaque stabilization. Based on the integrative medicine concept of brain-heart-kidney co-treatment and the shared pathophysiological mechanisms underlying DN progression and cardiovascular complications, Naoxintong Capsule represents a promising adjunctive therapy for DN.

STUDY DESIGN AND OBJECTIVES

This is a multicenter, randomized, double-blind, placebo-controlled clinical trial designed to provide high-level evidence for the efficacy and safety of Naoxintong Capsule in treating DN. The study will enroll 410 adult patients with confirmed Type 2 diabetic nephropathy across approximately 20 clinical centers in China.

The primary objective is to evaluate whether adding Naoxintong Capsule to standard conventional therapy can slow the annual rate of eGFR decline compared with standard therapy alone (with placebo). Secondary objectives include assessing effects on proteinuria, CKD stage progression, time to ESKD, cardiovascular events, traditional Chinese medicine (TCM) syndrome scores, and health-related quality of life.

PARTICIPANT POPULATION

Eligible participants are adults (age >= 18 years) with confirmed Type 2 diabetic nephropathy, 24-hour urinary protein excretion between 0.5 and 3.5 g, eGFR >= 45 mL/min/1.73m2, and on stable ACEI/ARB therapy for at least 8 weeks prior to enrollment. Patients must discontinue all other traditional Chinese medicine products for a washout period of at least 4 weeks before randomization.

INTERVENTION

Participants will be randomized (1:1) to receive either Naoxintong Capsules or matching placebo capsules, both administered as 4 capsules per dose, 3 times daily, taken orally 30 to 60 minutes after meals. All participants continue to receive standard conventional therapy for DN, including glycemic control, blood pressure management, lipid-lowering therapy, dietary management, and treatment of CKD-related complications as clinically indicated. The treatment duration is 12 months.

FOLLOW-UP AND ASSESSMENTS

Following randomization at Visit 1 (V1), participants will attend scheduled visits at Month 1 (V2), Month 3 (V3), Month 6 (V4), Month 9 (V5), and Month 12 (V6). At each visit, clinical assessments include physical examination, laboratory tests (urinalysis, 24-hour urine protein, urine albumin-to-creatinine ratio, complete blood count, blood biochemistry including renal function, HbA1c, lipid profile, hs-CRP, IL-6), ECG, TCM syndrome scoring, and adverse event monitoring. At selected visits (V1, V6), additional imaging studies (chest X-ray/CT, renal ultrasound) and optional fundoscopy are performed. Biological samples (blood, urine, stool) are collected at V1, V4, and V6 for exploratory analyses including gut microbiota and metabolomics.

SAMPLE SIZE

The sample size of 410 (205 per group) was calculated based on detecting a clinically meaningful difference of 1.0 mL/min/1.73m2/year in eGFR annual decline slope between groups (expected: -3.0 vs. -2.0 mL/min/1.73m2/year), with a pooled standard deviation of 3.2, at a two-sided alpha of 0.05 and 80% power, allowing for a 20% dropout rate.

STATISTICAL ANALYSIS

Efficacy analyses will be conducted on both the Full Analysis Set (FAS, intention-to-treat) and the Per-Protocol Set (PPS). The primary analysis will use a mixed-effects model for the eGFR slope, adjusting for center effect. Time-to-event outcomes will be analyzed using Kaplan-Meier methods and Cox proportional hazards models. Safety analyses will be performed on the FAS.

研究类型

介入性

注册 (估计的)

410

阶段

  • 第四阶段

联系人和位置

本节提供了进行研究的人员的详细联系信息，以及有关进行该研究的地点的信息。

学习联系方式

学习地点

  • 中国
    • Beijing Municipality
      • Beijing、Beijing Municipality、中国
        • China-Japan Friendship Hospital
        • 接触：
      • Beijing、Beijing Municipality、中国、100853
        • Chinese PLA General Hospital, First Medical Center
        • 接触：
    • Chongqing Municipality
      • Chongqing、Chongqing Municipality、中国
        • Daping Hospital, Army Medical University
        • 接触：
    • Liaoning
      • Dalian、Liaoning、中国
        • First Affiliated Hospital of Dalian Medical University
        • 接触：
    • Shanghai Municipality
      • Shanghai、Shanghai Municipality、中国
        • Renji Hospital, Shanghai Jiao Tong University School of Medicine
        • 接触：
      • Shanghai、Shanghai Municipality、中国
        • Ruijin Hospital, Shanghai Jiao Tong University School of Medicine
        • 接触：
      • Shanghai、Shanghai Municipality、中国
        • Longhua Hospital, Shanghai University of Traditional Chinese Medicine
        • 接触：
    • Zhejiang
      • Hangzhou、Zhejiang、中国
        • Zhejiang Provincial Hospital of Traditional Chinese Medicine
        • 接触：

参与标准

研究人员寻找符合特定描述的人，称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

  • 成人
  • 年长者

接受健康志愿者

不

描述

Inclusion Criteria:

  1. Age >= 18 years.

  2. Meets the diagnostic criteria for Type 2 diabetic nephropathy, defined as:

    1. Confirmed diagnosis of Type 2 diabetes mellitus; AND
    2. At least one of the following: urinary albumin-to-creatinine ratio (UACR) >= 30 mg/g, or eGFR < 60 mL/min/1.73m^2, confirmed by repeat testing (interval >= 3 months), after excluding transient factors such as acute kidney injury, dehydration, infection, or heart failure; OR
    3. Renal biopsy confirmed as isolated diabetic nephropathy; AND
    4. Exclusion of other primary or secondary kidney diseases.
  3. 24-hour urinary protein excretion >= 0.5 g and < 3.5 g.
  4. Estimated glomerular filtration rate (eGFR) >= 45 mL/min/1.73m^2.
  5. On a stable dose of ACE inhibitor (ACEI) or Angiotensin II receptor blocker (ARB) therapy for at least 8 weeks prior to enrollment. If SGLT2 inhibitors, mineralocorticoid receptor antagonists (MRA), or GLP-1 receptor agonists are being used, the dose must have been stable for at least 4 weeks prior to enrollment and remain unchanged during the study period. Patients not currently using these agents must not initiate them during the study.
  6. Signed informed consent form.

Exclusion Criteria:

  1. Type 1 diabetes mellitus or other types of diabetes mellitus (e.g., secondary diabetes, maturity-onset diabetes of the young).
  2. Coexisting systemic autoimmune or immune-mediated disease where the clinical assessment suggests a non-diabetic nephropathy etiology.
  3. Decline in eGFR of > 30% within the past 3 months.
  4. Persistent serum potassium > 5.5 mmol/L.
  5. Diagnosis of hemorrhagic cardiovascular or cerebrovascular disease within the past 3 months.
  6. Known allergy or hypersensitivity to any component of Naoxintong Capsule or placebo; pregnant or lactating women.
  7. Participation in another drug or medical device clinical trial within the past 6 months.
  8. Any other condition that, in the investigator's judgment, renders the patient unsuitable for participation in the clinical trial (e.g., severe hepatic dysfunction, life expectancy < 1 year).

学习计划

本节提供研究计划的详细信息，包括研究的设计方式和研究的衡量标准。

研究是如何设计的？

设计细节

  • 主要用途：治疗
  • 分配：随机化
  • 介入模型：并行分配
  • 屏蔽：双倍的

武器和干预

参与者组/臂
干预/治疗
实验性的：Naoxintong Capsule Group
Participants will receive Naoxintong Capsules (4 capsules per dose, 3 times daily, orally, 30-60 minutes after meals) in addition to standard conventional therapy for diabetic nephropathy, for a total treatment duration of 12 months. Standard conventional therapy includes glycemic control (oral hypoglycemic agents and/or insulin), blood pressure management (ACEI or ARB, with optional non-RASI antihypertensives), lipid-lowering therapy (statins as indicated), dietary management (protein 0.6-0.8 g/kg/day, sodium <3 g/day), and treatment of CKD-related complications as clinically indicated.
药品：Naoxintong Capsule
Naoxintong Capsule is a traditional Chinese medicine formulation composed of 16 herbal and animal-derived ingredients: Astragalus membranaceus (Huangqi), Prunus persica seed (Taoren), Carthamus tinctorius flower (Honghua), Paeonia lactiflora root (Chishao), Angelica sinensis root (Danggui), Ligusticum chuanxiong rhizome (Chuanxiong), Boswellia carterii resin (Ruxiang), Commiphora myrrha resin (Moyao), Salvia miltiorrhiza root (Danshen), Achyranthes bidentata root (Niuxi), Cinnamomum cassia twig (Guizhi), Morus alba twig (Sangzhi), Spatholobus suberectus stem (Jixueteng), Buthus martensii (Quanxie), Pheretima aspergillum (Dilong), and Hirudo nipponica (Shuizhi). Each capsule contains 0.4 g of active ingredients. Dosage: 4 capsules (1.6 g) per dose, taken orally 3 times daily, 30-60 minutes after meals. Manufactured by Shaanxi Buchang Pharmaceutical Co., Ltd. (National Drug Approval No.: Guoyaozhunzi Z20025001). Storage: sealed, at room temperature. Shelf life: 24 months.
安慰剂比较：Placebo Group
Participants will receive matching placebo capsules (4 capsules per dose, 3 times daily, orally, 30-60 minutes after meals) in addition to standard conventional therapy for diabetic nephropathy, for a total treatment duration of 12 months. Standard conventional therapy is identical to that provided in the Naoxintong group.
药品：Placebo
Matching placebo capsules identical in appearance, size, shape, color, weight, packaging, and labeling to Naoxintong Capsules but containing no active pharmaceutical or herbal ingredients. Dosage: 4 capsules per dose, taken orally 3 times daily, 30-60 minutes after meals. Manufactured by Shaanxi Buchang Pharmaceutical Co., Ltd. Storage: sealed, at room temperature. Shelf life: 24 months.

研究衡量的是什么？

主要结果指标

结果测量
措施说明
大体时间
Annual Rate of Decline in Estimated Glomerular Filtration Rate (eGFR)
大体时间：Baseline to Month 12
The annual rate of decline in eGFR (ml/min/1.73m^2/year), calculated as the slope of eGFR over the 12-month treatment period using all available eGFR measurements at each scheduled visit. eGFR is estimated using the CKD-EPI equation. A less negative slope indicates slower disease progression.
Baseline to Month 12
Change in 24-Hour Urinary Protein Excretion From Baseline
大体时间：Baseline to Month 12
Change from baseline in 24-hour urinary protein excretion (g/24h), measured at each scheduled visit. A decrease indicates renal protective effect.
Baseline to Month 12
Renal Composite Endpoint: eGFR Decline >30%, ESKD, or MACE
大体时间：From randomization through Month 12
Time to first occurrence of: sustained eGFR decline >30% from baseline; end-stage kidney disease; or major adverse cardiovascular event.
From randomization through Month 12

次要结果测量

结果测量
措施说明
大体时间
Proportion of Participants With CKD Stage Improvement, Stabilization, or Progression
大体时间：Baseline to Month 12
Proportion of participants whose CKD stage (KDIGO eGFR categories) improved, remained stable, or progressed.
Baseline to Month 12
Time to Sustained eGFR Decline of Greater Than 30% From Baseline
大体时间：From randomization through Month 12
Time from randomization to first confirmed sustained eGFR decline exceeding 30% from baseline.
From randomization through Month 12
Time to End-Stage Kidney Disease (ESKD)
大体时间：From randomization through Month 12
Time from randomization to ESKD: maintenance dialysis, kidney transplantation, or sustained eGFR <15.
From randomization through Month 12
Time to First Unplanned Hospitalization for Heart Failure
大体时间：From randomization through Month 12
Time from randomization to first unplanned hospital admission primarily due to heart failure.
From randomization through Month 12
Time to First Non-Fatal Myocardial Infarction
大体时间：From randomization through Month 12
Time from randomization to first non-fatal MI per WHO-MONICA criteria.
From randomization through Month 12
Time to First Non-Fatal Ischemic Stroke
大体时间：From randomization through Month 12
Time from randomization to first non-fatal ischemic stroke with imaging confirmation.
From randomization through Month 12
Time to Cardiovascular Death or Stroke-Related Death
大体时间：From randomization through Month 12
Time from randomization to death attributable to cardiovascular or cerebrovascular causes.
From randomization through Month 12
Time to All-Cause Death
大体时间：From randomization through Month 12
Time from randomization to death from any cause.
From randomization through Month 12
Change in TCM Syndrome Score From Baseline
大体时间：Baseline to Month 12
Change in TCM syndrome score using a standardized 90-item questionnaire.
Baseline to Month 12

合作者和调查者

在这里您可以找到参与这项研究的人员和组织。

赞助

Chen Xiangmei

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查，以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (估计的)

2027年3月1日

初级完成 (估计的)

2028年6月1日

研究完成 (估计的)

2028年12月30日

研究注册日期

首次提交

2026年7月8日

首先提交符合 QC 标准的

2026年7月8日

首次发布 (实际的)

2026年7月13日

研究记录更新

最后更新发布 (实际的)

2026年7月13日

上次提交的符合 QC 标准的更新

2026年7月8日

最后验证

2026年7月1日

更多信息

与本研究相关的术语

关键字

其他相关的 MeSH 术语

其他研究编号

  • NXT-DKD-2026-001

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)？

是的

IPD 计划说明

De-identified individual participant data (IPD) may be shared with qualified researchers upon reasonable request, subject to a data use agreement, following publication of the primary results.

IPD 共享时间框架

After publication of primary results

IPD 共享访问标准

Via reasonable request with data use agreement

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索，没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求，请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改，我们的网站上也会自动更新.

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