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临床试验/NCT02982876
NCT02982876已完成不适用

Airway Stents for Excessive Dynamic Airway Collapse: A Randomized Controlled Trial

Beth Israel Deaconess Medical Center0 个研究点目标入组 50 人开始时间: 2016年12月1日最近更新:
适应症

试验速览

阶段
不适用
状态
已完成
入组人数
50
主要终点
St. George's Respiratory Questionnaire

研究概览

简要总结

Airway stents are used as standard of care to identify which patients with excessive dynamic airway collapse will benefit from a definitive surgical treatment. However, the specific way in which these stents are effective has not been tested. The purpose of this research study is to determine the effectiveness of airway stents when used in the airways of patients with severe symptomatic excessive dynamic airway collapse compared to patients with severe symptomatic excessive dynamic airway collapse that do not receive airway stent.

详细描述

Study Design

This randomized controlled trial will be conducted at Beth Israel Deaconess Medical Center (BIDMC) in accordance with Good Clinical Practice Standards and under IRB supervision. We plan to enroll total of 48 patients with EDAC randomized by a computer generated system to either intervention group (airway stent) or medical management group.

Description of the study

Previous to appointment all patients will have Airway CT scan, 6 minute walk test and pulmonary function test as per protocol and standard of care.

Enrollment

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

  • Patient with sever symptomatic EDAC (collapse >90% of the airway during exhalation at dynamic CT scan)
  • Age > 18 years

排除标准

  • Patients who have not been well managed from their respiratory comorbidities (asthma, COPD, obstructed sleep apnea, GERD, relapsing polychondritis)
  • Current respiratory infection
  • Resting bradycardia (<50 beats/min), frequent multifocal PVCs, complex ventricular arrhythmia, sustained SVT
  • Dysrhythmia that might pose a risk during exercise or training
  • Any disease or condition that interferes with completion of initial or follow-up assessments

结局指标

主要结局

St. George's Respiratory Questionnaire

时间窗: 7-14 days

Index designed to measure health status in patients with respiratory symptoms

次要结局

  • Peak flow(7-14 days)
  • 6 minute walk test(7-14 days)
  • FEV1(7-14 days)
  • Cough Quality of life Questionnaire(7-14 days)
  • Self-reported symptoms(7-14 days)
  • modified Medical Research Council scale of dyspnea(7-14 days)
  • Complications(7-14 days)

研究者

申办方类型
Other
责任方
Principal Investigator
主要研究者

Adnan Majid, MD

MD

Beth Israel Deaconess Medical Center

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