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临床试验/NCT07709871
NCT07709871尚未招募不适用

A Prospective Study On The Effect Of Oral Chelator Therapy On Delaying Renal Function Progression In Type 2 Diabetic Nephropathy Patients With Elevated Lead Burden

The Fourth Affiliated Hospital of Zhejiang University School of Medicine0 个研究点目标入组 42 人开始时间: 2026年8月1日最近更新:
适应症
相关药物

试验速览

阶段
不适用
状态
尚未招募
发起方
入组人数
42
主要终点
Change in estimated glomerular filtration rate (eGFR) from baseline at 12 months after oral chelation therapy

研究概览

简要总结

This is a single-arm prospective clinical study conducted at The Fourth Affiliated Hospital of Zhejiang University School of Medicine. Previous basic research has found that patients with type 2 diabetic nephropathy have higher blood lead levels than ordinary people, and lead accumulation may accelerate kidney function decline. A total of 42 eligible participants will be enrolled, who are diagnosed with type 2 diabetic nephropathy, have baseline blood lead ≥5 µg/dl, CKD stage ≤3 and 24-hour urinary protein <8 g. All subjects will receive oral dimercaptosuccinic acid (DMSA) capsules for lead removal according to standardized treatment courses for up to 3 months. During treatment, blood lead, urine lead, renal function and other indicators will be tested monthly. After the 3-month intervention, all participants will be followed up for 12 months, with relevant laboratory examinations conducted every 3 months to observe changes in renal function. The main goal of this study is to evaluate whether oral lead chelation therapy can slow the progression of kidney damage in patients with high lead burden and type 2 diabetic nephropathy, and provide clinical evidence for the intervention of lead-induced kidney injury in diabetic populations. Patients with hypertension, hyperlipidemia, autoimmune diseases, malignant tumor history, previous occupational lead exposure or drug allergies will not be enrolled. No healthy volunteers will be recruited, and individual raw patient data will not be shared externally after the study.

研究设计

研究类型
Interventional
分配方式
Na
干预模型
Single Group
主要目的
Treatment
盲法
None

入排标准

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

入选标准

  • Diagnosed with type 2 diabetic nephropathy;
  • Baseline blood lead level ≥ 5 μg/dL;
  • Chronic kidney disease stage ≤ 3;
  • 24-hour urinary protein < 8 g;
  • Age ≥ 18 years;
  • Able to voluntarily sign a written informed consent form.

排除标准

  • Combined hypertension or hyperlipidemia;
  • Confirmed history of autoimmune diseases;
  • Personal history of malignant tumors;
  • Reversible renal insufficiency (malignant hypertension, active urinary tract infection, recent use of nephrotoxic drugs);
  • Previous occupational lead exposure history;
  • Known drug allergy to dimercaptosuccinic acid;
  • Unable to complete regular follow-up visits.

结局指标

主要结局

Change in estimated glomerular filtration rate (eGFR) from baseline at 12 months after oral chelation therapy

时间窗: 3 months oral chelation intervention, followed by 12 months of quarterly follow-up assessment, with the primary endpoint measured at the 12-month post-treatment visit

次要结局

未报告次要终点

研究者

发起方
The Fourth Affiliated Hospital of Zhejiang University School of Medicine
申办方类型
Other
责任方
Sponsor

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