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临床试验/NCT02555319
NCT02555319已完成不适用

A Feasibility Study to Evaluate the Safety and Short-term Effectiveness of Implantation of Transcatheter Pulmonary Valve (TPV) for the Treatment of Congenital Heart Disease With Pulmonary Valve Disease

Seoul National University Hospital1 个研究点 分布在 1 个国家目标入组 10 人开始时间: 2015年8月26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
入组人数
10
试验地点
1
主要终点
Procedural success

研究概览

简要总结

The purpose of this study is to evaluate the safety and short-term effectiveness of implantation of Transcatheter Pulmonary Valve (TPV) for the treatment of congenital heart disease with pulmonary valve disease.

详细描述

Diverse congenital heart diseases involving the pulmonary artery, such as Tetralogy of Fallot (TOF) with or without pulmonary atresia, or transposition of the great arteries with pulmonary stenosis, require implantation of an artificial conduit between the right ventricle and the pulmonary artery(PA). Because these conduits finally degenerate and result in pulmonary regurgitation and/or stenosis and progressive right ventricle (RV) dilation and eventual failure, patients need repetitive surgery for conduit revision. Transcatheter pulmonary valve implantation (TPVI) is a less invasive alternative to surgery in patients with dysfunctional right ventricular outflow tract (RVOT). TPV is a large-diameter (up to 28 mm) self-expandable stent with a relatively low profile from a nitinol wire backbone with valve leaflets made from porcine pericardial tissue. The TPV is indicated for use in patients with previous undergone replacement of bioprosthetic valve or conduit due to either pulmonary valve atresia, stenosis, regurgitation or a combination of them and present with dysfunctional RVOT requiring treatment for severe pulmonary regurgitation and/or RVOT conduit obstruction. Consecutive subject data should be collected at discharge, 1, 3, 6 month, and 1-5 years post TPV implantation.

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
10 Years 至 —(Child, Adult, Older Adult)
性别
All
接受健康志愿者
否

入选标准

  • •Age greater than or equal to 10 years of age
  • •Body weight greater than or equal to 30 kilograms
  • •Pulmonary regurgitation ≥moderate pulmonary regurgitation (PR) (≥3+) or RVOT conduit obstruction with mean gradient >35mmHg by echocardiography
  • •pulmonary artery annulus or in situ conduit size ≥16 and ≤26mm
  • •Patient willing to provide written informed consent and comply with follow-up requirements

排除标准

  • •Pre-existing mechanical heart valve in any position
  • •Obstruction of the central veins (pulmonic bioprosthesis delivery system to the heart)
  • •Coronary artery compression
  • •A known hypersensitivity to Aspirin or Heparin
  • •Immunosuppressive disease
  • •Active infectious disease (e.g. endocarditis, meningitis)
  • •Estimated survival less than 6 months
  • •Female of child-bearing potential who are unable to take adequate contraceptive precautions, are known to be pregnant, or are currently breastfeeding an infant.

研究组 & 干预措施

Transcatheter Pulmonary Valve

Experimental

Transcatheter Pulmonary Valve (TaeWoong Medical Co., Ltd. Korea)

干预措施: Transcatheter Pulmonary Valve (TPV) (Device)

结局指标

主要结局

Procedural success

时间窗: 5day

Procedural success is defined as the TPV implant within desired position, RV-PA peak systolic pressure gradient \<35mmHg by catheter, less mild pulmonary regurgitation by angiography, and freedom from explantation of the TPV at 24 hours post-implant.

Hemodynamic functional improvement at 6month

时间窗: 6 month

Hemodynamic functional improvement is defined as mean RVOT gradient ≤30 mmHg by continuous wave doppler, and a pulmonary regurgitant fraction \<20% by cardiac magnetic resonance (MR).

Procedural / Device related serious adverse events at 6month

时间窗: 6 month

次要结局

  • Severity of pulmonary regurgitation(5year)
  • Pulmonary regurgitant fraction(5year)
  • New York Heart Association (NYHA) functional classification(5 year)
  • Stent fracture(5 year)
  • Death (all cause / procedural / device-related)(5 year)
  • Other adverse events(5 year)
  • Hemodynamic function(5 year)
  • Catheter reintervention on TPV(5 year)
  • Reoperation(5 year)
  • Procedural / Device related serious adverse events(5 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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