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临床试验/NCT07009938
NCT07009938尚未招募不适用

Long-Term Efficacy and Safety of Drug-Coated Balloon Angioplasty in Patients With Coronary Artery Disease and Type 2 Diabetes: A Multicenter, Prospective, Randomized Controlled Trial

Shanghai 10th People's Hospital6 个研究点 分布在 1 个国家目标入组 1,000 人开始时间: 2025年7月1日最近更新:
适应症
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
1,000
试验地点
6
主要终点
Target Lesion Diameter Stenosis Rate

研究概览

简要总结

Patients with coronary artery disease (CAD) and type 2 diabetes mellitus (T2DM) often present with diffuse, complex lesions and a higher risk of in-stent restenosis after PCI. While drug-eluting stents (DES) remain the standard treatment, their long-term efficacy in diabetic patients is suboptimal. Drug-coated balloons (DCBs) offer a "leave nothing behind" strategy by delivering anti-proliferative drugs without permanent implants, potentially reducing restenosis and adverse events. Although DCBs have shown promise in selected lesion types, evidence in T2DM patients is limited, particularly from prospective, randomized trials. This study aims to evaluate the efficacy and safety of DCB angioplasty compared to conventional strategies in patients with CAD and T2DM, focusing on angiographic outcomes, symptom relief, and major adverse cardiovascular events.

详细描述

Coronary artery disease (CAD) and type 2 diabetes mellitus (T2DM) often coexist, and the long-term hyperglycemic state and metabolic disorders in diabetic patients contribute to endothelial dysfunction and accelerated atherosclerosis. As a result, coronary lesions in T2DM patients tend to be more diffuse and complex, posing greater challenges to percutaneous coronary intervention (PCI). Although drug-eluting stents (DES) have significantly improved clinical outcomes, diabetic patients remain at higher risk for in-stent restenosis (ISR) and target lesion revascularization (TLR), negatively impacting long-term prognosis.

Drug-coated balloons (DCBs), a novel PCI technique, allow for rapid and effective delivery of anti-proliferative agents (e.g. paclitaxel or sirolimus) to the vessel wall without leaving behind a permanent implant. This "leave nothing behind" approach reduces the risk of chronic inflammation and stent-related complications. DCBs have shown promising results in non-diabetic populations, particularly in small vessel disease and bifurcation lesions. However, evidence supporting their use in T2DM patients remains limited, especially from prospective, randomized controlled trials. As such, whether DCBs can serve as a viable alternative to DES in this high-risk group remains an open question.

This study aims to evaluate the efficacy and safety of DCB angioplasty in patients with CAD and T2DM through a prospective, randomized controlled design. The study will focus on restenosis rates, improvement in angina symptoms, incidence of major adverse cardiovascular events (MACE), and patient-reported quality of life outcomes, providing a more individualized and evidence-based treatment approach for this challenging patient population.

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
Single (Participant)

入排标准

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

入选标准

  • •Age ≥18 years
  • •Diagnosed CAD with ≥70% stenosis in ≥1 coronary artery confirmed by coronary angiography
  • •Diagnosed type 2 diabetes (per WHO criteria)
  • •Target lesion suitable for DCB (diameter 2.0-4.0 mm, length ≤40 mm)
  • •Informed consent provided

排除标准

  • •Prior coronary artery bypass surgery or PCI with complications
  • •STEMI within 24 hours
  • •Severe hepatic/renal dysfunction
  • •Active bleeding or uncontrolled anticoagulation
  • •Allergy to DCB components
  • •Pregnancy or lactation
  • •Psychiatric conditions limiting compliance

研究组 & 干预措施

Percutaneous coronary intervention using Drug-Coated Balloon (DCB)

Experimental

Percutaneous coronary intervention using Drug-Coated Balloon (DCB)

干预措施: Drug-Coated Balloon (DCB) (Device)

Either Drug-Eluting Stent (DES) implantation group

Active Comparator

Percutaneous coronary intervention using Drug-Eluting Stent (DES) implantation

干预措施: Drug-Eluting Stent (DES) implantation (Device)

结局指标

主要结局

Target Lesion Diameter Stenosis Rate

时间窗: At 12 months after intervention

Target Lesion Diameter Stenosis Rate refers to the percentage of narrowing at the target coronary lesion, calculated by comparing the minimal lumen diameter (MLD) at the lesion site with the reference vessel diameter (RVD), which was measured based on coronary angiography.

次要结局

  • Glycemic indices(At 3, 6 and 12 months after intervention)
  • Major Adverse Cardiovascular Events (MACE)(At 12 months after intervention)
  • Angina Symptom Improvement(At baseline, 1, 3, 6 and 12 months after intervention)
  • Changes in glycemic indices including glycated hemoglobin (HbA1c)(At 3, 6 and 12 months after intervention)

研究者

发起方
Shanghai 10th People's Hospital
申办方类型
Other
责任方
Principal Investigator
主要研究者

Ya-Wei Xu

Chief Physician

Shanghai 10th People's Hospital

研究点 (6)

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