跳至主要内容
临床试验/NCT04206852
NCT04206852招募中不适用

Safety and Efficacy of Balloon Pulmonary Angioplasty in China

Chinese Pulmonary Vascular Disease Research Group2 个研究点 分布在 1 个国家目标入组 200 人开始时间: 2018年5月11日最近更新:
适应症

试验速览

阶段
不适用
状态
招募中
发起方
入组人数
200
试验地点
2
主要终点
Change of cardiac index (CI) in L/m^2 caused by series of BPA.

研究概览

简要总结

Balloon pulmonary angioplasty (BPA) is a potential treatment for non-operable patients with chronic thromboembolic pulmonary hypertension (CTEPH).

The aim of this study was to evaluate the safety and efficacy of BPA in CTEPH patients not amenable to pulmonary endarterectomy(PEA) or suffered from persistent CTEPH after PEA.

详细描述

This study is a prospective, multi-center, long-term observational project to study the safety and efficacy of BPA. Clinical evaluation, including: functional capacity, 6-minutes walking test, biomarkers, cardiopulmonary exercise test, electrocardiography, echocardiography, haemodynamics, pulmonary angiography and lung scintigraphy was performed before the initiation therapy of BPA, and 3-12 months after last session of BPA.

we also aim to evaluate the value of FAPI in predicting the efficacy and the prognosis of patients with CTEPH who received BPA.

研究设计

研究类型
Observational
观察模型
Cohort
时间视角
Prospective

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 CTEPH according to ESC Guidelines (1) Mean PAP ≥ 25mmHg at rest; or if mean PAP < 25mmHg at rest, have exercise limitations from chronic thromboembolic disease (2)Abnormal ventilation perfusion lung scanning (VQ) scan, pulmonary angiogram, computer tomographic pulmonary angiogram, or magnetic resonance pulmonary angiogram confirming chronic thromboembolic disease as recommended by standard guidelines
  • Treatment with anticoagulation for ≥ 3 months before diagnosis of CTEPH
  • Not amenable to pulmonary endarterectomy
  • Willing to provide informed consent

排除标准

  • Patients unwilling or unable to provide written consent for participation in the study.
  • Impossible to follow up.

结局指标

主要结局

Change of cardiac index (CI) in L/m^2 caused by series of BPA.

时间窗: From initiation of BPA to 3-12 months after last session

Cardiac index (CI) in L/m\^2 is obtained by right cardiac catheterization.

Change of diffusing capacity for carbon monoxide caused by series of BPA.

时间窗: From initiation of BPA to 3-12 months after last session

diffusing capacity for carbon monoxide in % is obtained from pulmonary function test

Change of Pulmonary vascular resistance (PVR) in Wood U caused by series of BPA.

时间窗: From initiation of BPA to 3-12 months after last session

Pulmonary vascular resistance (PVR) in Wood U is obtained by right cardiac catheterization.

Change of N-terminal B-type natriuretic peptide in pg/ml caused by series of BPA.

时间窗: From initiation of BPA to 3-12 months after last session

World Health Organization is obtained from electronic medical records.

Change of World Health Organization (WHO) functional capacity classification caused by series of BPA.

时间窗: From initiation of BPA to 3-12 months after last session

World Health Organization is obtained from electronic medical records.

Incidence of Treatment-Emergent Adverse Events of BPA procedure.

时间窗: From initiation of BPA to 3-12 months after last session

Surveillance of complications including: vessel injury, desaturation, cough, mild hemoptysis (\<50ml), severe hemoptysis (\>50ml), reperfusion pulmonary injury, death.

Change of Pulmonary artery pressure in mmHg caused by series of BPA.

时间窗: From initiation of BPA to 3-12 months after last session

Pulmonary artery pressure in mmHg is obtained by right cardiac catheterization.

Change of six minutes walk distance in meter caused by series of BPA.

时间窗: From initiation of BPA to 3-12 months after last session

World Health Organization is obtained from electronic medical records.

Change of Peak VO2/kg in ml/min/kg caused by series of BPA.

时间窗: From initiation of BPA to 3-12 months after last session

Peak VO2/kg in ml/min/kg is obtained by cardiopulmonary exercise test.

Change of fibroblast activation protein inhibitor expression after BPA

时间窗: From initiation of BPA to 3-12 months after last session

Change of fibroblast activation protein inhibitor expression after BPA

次要结局

未报告次要终点

研究者

发起方
Chinese Pulmonary Vascular Disease Research Group
申办方类型
Other
责任方
Sponsor

研究点 (2)

Loading locations...

相似试验