ISAR-DESIRE 4: Randomized Trial Of Scoring Balloon in Patients With Restenosis in "Limus"-Eluting Coronary Stents Undergoing Angioplasty With Paclitaxel-Coated Balloon
试验速览
- 阶段
- 4 期
- 状态
- 已完成
- 发起方
- 入组人数
- 252
- 试验地点
- 2
- 主要终点
- In-segment percent diameter stenosis
研究概览
简要总结
The purpose of the study is to determine whether scoring balloon (SCB) plus paclitaxel-coated balloon (PCB) is superior to PCB alone for the treatment of restenosis within "limus"-eluting stents (LES)
详细描述
The optimal treatment of in-BMS-restenosis seems to be implantation of a DES which is supported by a large body of evidence. Nevertheless, several recent published studies have shown a substantial reduction in late lumen loss and angiographic restenosis using paclitaxel-coated balloons (PCB) for restenotic lesions. Given the increased world-wide use of DES and the use of DES in increasingly complex coronary disease patterns, the number of patients presenting with restenosis after DES implantation will further increase in the coming decade.
Data regarding the optimal treatment of in-DES-restenosis are very limited: Implanting a new DES for in-DES-restenosis has been reported to associate with repeat restenosis rates as high as 20%. In addition, an increased risk of stent thrombosis has been associated with complex stenting and with additional DES implantation. Thus, for lesions which develop restenosis after LES implantation, the optimal treatment strategy remains unknown.
Few results on small sample-size populations have been reported in patients treated with scoring or cutting balloon (SCB) technology for treatment of BMS restenosis as compared to plain balloon angioplasty. Moreover, the efficacy of SCB angioplasty in DES restenosis has not been adequately addressed. Furthermore, the potential additive benefit of SCB angioplasty in patients undergoing PCB therapy remains to be elucidated. The hypothesis behind this concept is that the application of SCB prior to deployment of PCB may increase the bioavailability of paclitaxel within the restenotic tissue, and therefore may increase the efficacy of PCB. There are numerous preclinical studies to support this hypothesis, which show that lesion preparation is an important pre-requisite for the effectiveness of PCB.
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
- 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
- 否
入选标准
- •Patients with ischemic symptoms or evidence of myocardial ischemia in the presence of ≥ 50% restenosis after prior implantation of LES in native coronary vessels.
- •Written, informed consent by the patient or her/his legally-authorized representative for participation in the study.
- •In women with childbearing potential a negative pregnancy test is mandatory.
排除标准
- •Age < 18 years
- •Cardiogenic shock
- •Acute ST-elevation myocardial infarction within 48 hours from symptom onset.
- •Malignancies or other comorbid conditions (for example severe liver, renal and pancreatic disease) with life expectancy less than 12 months or that may result in protocol non-compliance.
- •Severe renal insufficiency (glomerular filtration rate ≤ 30 ml/min)
- •Contraindications to antiplatelet therapy, paclitaxel, stainless steel, cobalt, chrome
- •Therapy including Lovastatin, Ciclosporin, Terfenadine, Midazolam, or Ondansetron
- •Pregnancy (present, suspected or planned) or positive pregnancy test.
- •Previous enrollment in this trial.
- •Patient's inability to fully comply with the study protocol.
研究组 & 干预措施
Paclitaxel Eluting Balloon + Scoring Balloon
Dilatation of the lesion with an Paclitaxel Eluting Balloon before the utilization of a Scoring Balloon
干预措施: Paclitaxel Eluting Balloon + Scoring Balloon (Device)
Paclitaxel Eluting Balloon
Paclitaxel Eluting Balloon
干预措施: Paclitaxel Eluting Balloon (Device)
结局指标
主要结局
In-segment percent diameter stenosis
时间窗: 6-8 months
In-segment percent diameter stenosis (%DS) at 6-8 month follow-up angiography
次要结局
- In-stent late lumen loss(6-8 months)
- Target lesion thrombosis(1 and 2 years)
- In-segment binary angiographic restenosis(6-8 month)
- Death or myocardial infarction(1 and 2 years)
- Target lesion revascularization(1 and 2 years)
- OCT tissue characterization(6-8 months)
