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临床试验/NCT01722799
NCT01722799已完成不适用

PROSPECTIVE RANDOMIZED TRIAL Multicentric Study to Evaluate the Treatment and the Efficiency of Paclitaxel-coated Balloon IN.PACT FALCON ® in Small-vessel Coronary Stenosis.

Andres Iñiguez Romo, MD, PhD2 个研究点 分布在 1 个国家目标入组 97 人开始时间: 2012年12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
已完成
发起方
入组人数
97
试验地点
2
主要终点
Compare the clinical security measured by the incidence MACE of DEB IN.PACT FALCON DEB versus the resolute integrity stent (DES).

研究概览

简要总结

Significant lesions in small coronary arteries are frequently found (35%-50%) in patients with coronary artery disease. Independently of the type of coronary angioplasty the restenosis and the need for repeat revascularization remains the main limitation, representing a challenging problem even in the DES (drug eluting stent) era. Recently has been developed drug eluting balloons (DEBs), which have been successfully tested in small series on in-stent restenosis, but few evidence is available in the context of small vessels disease.

The current study has been designed to know, in one hand, the clinical efficacy of the Drug elluting balloon IN.PACT FALCON and, in other hand, the effectiveness, and the cost-effectiveness incremental analysis of DEBs (IN.PACT FALCON vs. DES ( RESOLUTE INTEGRITY) in patients with de novo lesions in small vessels.

详细描述

Recent studies have reported the efficacy of the local application of paclitaxel ® inhibiting neointimal proliferation, and thus the limitation of restenosis, which has led to the conception and development of drug-coated balloon or "Drug Eluting Balloons" (DEB), releasing the antiproliferative drug at the time of expansion. Initially they were applied in the treatment of in-stent restenosis. However, DEB may represent a therapeutic alternative in other contexts where anatomo-clinical uses are not always therapeutic percutaneous coronary revascularization with stent implantation, as is the case of coronary lesions located in small vessels.

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

入选标准

  • Older than 18, informed consent.
  • Evidence of CAD with severe de novo lesion in the native coronary arteries ( ≥70% stenosis by visual estimation or >50% by CT scan); affecting
  • Vessels between 2,25 and 2,75 mm diameter and
  • The length of the coronary stenosis ≤25 mm
  • Patient informed consent form signed.

排除标准

  • Lesion in coronary left main ,
  • Chronic total occlusions,
  • Lesions at bifurcation,
  • Severe calcified lesions,
  • Lesions in aorto-coronary saphenous veins or arterial grafts,
  • Acute Myocardial Infarction during 48 hours before the procedure,
  • Severe renal dysfunction,
  • Hypersensibility, allergy or contraindication of medication: acetylsalicylic acid, clopidogrel, ticlopidine, heparin, paclitaxel,
  • Allergy to contrast media,
  • Life expectancy less than 1 year,
  • 1 year FU not guaranteed,
  • Being participating in another study.

研究组 & 干预措施

Drug elluting Balloon (DEB)

Experimental

Is a coronary dilating device with Paclitaxel ® drug delivery, for dilatation and provisional spot bare metal stenting (BMS).

干预措施: Drug elluting Balloon (DEB) (Device)

Drug elluting coronary stent (DES)

Active Comparator

The Resolute Integrity Zotarolimus-Eluting Coronary Stent System is indicated for improving coronary luminal diameters in patients, including those with diabetes mellitus, with symptomatic ischemic heart disease due to de novo lesions of length ≤ 27 mm in native coronary arteries with reference vessel diameters of 2.25 mm to 4.20 mm.

干预措施: Drug elluting coronary stent (DES) (Device)

结局指标

主要结局

Compare the clinical security measured by the incidence MACE of DEB IN.PACT FALCON DEB versus the resolute integrity stent (DES).

时间窗: The security will be evaluated at one month, sixth month and one year

Rate of major adverse cardiac events (MACE) at 30 days, 6 months and one year. MACE was defined as cardiac death, myocardial infarction (MI) (with or without Q-wave), need for repeat revascularization of the treated vessel (surgical or repeat PCI) or occlusion of the treated lesion.

Compare the clinical efficacy measured by target vessel failure of DEB IN.PACT FALCON DEB versus the resolute integrity stent (DES).

时间窗: The efficacy will be evaluated at 1 year.

Target vessel failure (TVF) is define as any revascularization motivated due to myocardial infarction (with or without Q wave) or cardiac death related to the target vessel.

次要结局

  • Compare the efficiency of DEBs versus DES. in terms of cost effectiveness (cost per adverse event-death avoided) and cost-utility ( cost per quality adjusted life year) in patients with de novo lesions in small vessels.(The efficiency will be evaluated at first month, 6 month and 1 year.)
  • Compare the direct cost, indirect costs and total costs of DEBs versus DES in patients with de novo lesions in small vessels.(This outcome will be evaluated at first month, 6 month and 1 year.)

研究者

发起方
Andres Iñiguez Romo, MD, PhD
申办方类型
Other Gov
责任方
Sponsor Investigator
主要研究者

Andres Iñiguez Romo, MD, PhD

Dr. Andres Iñiguez Romo

Hospital de Meixoeiro

研究点 (2)

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