跳至主要内容
临床试验/NCT00972868
NCT00972868撤回不适用

Use of a Novel Unidirectional Face Mask During Noninvasive Positive Pressure Ventilation (NPPV) in Chronic Obstructive Pulmonary Disease (COPD) Patients

Massachusetts General Hospital2 个研究点 分布在 1 个国家开始时间: 2011年3月最近更新:
适应症

试验速览

阶段
不适用
状态
撤回
试验地点
2
主要终点
Reduction in anatomical dead space and improvement in ventilatory efficiency

研究概览

简要总结

The purpose of this study is to determine the feasibility, safety and efficacy of a unidirectional breathing mask (breathe in through the nose and out through the mouth or breathe in through the mouth and out through the nose) in COPD patients with breathing difficulties requiring noninvasive positive pressure ventilation (NPPV).

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

入选标准

  • Acute hypercapnic respiratory failure as a result of an acute exacerbation of COPD defined as PaCO2 > 50 mmHg, with or without hypoxia, and a respiratory rate of greater than 25/min with the use of accessory muscles of respiration or abdominal paradox;
  • Requiring NPPV as assessed by the managing care team.

排除标准

  • Patients with facial deformity, heavy beard or moustache which prevents a good seal between the mask and the face;
  • Patients who have claustrophobia and cannot wear the mask;
  • Patients who are hemodynamically unstable;
  • Patients who are disoriented and unable to cooperate with the study procedure;
  • DNI or DNR status or patients in whom intubation is contraindicated;
  • Patients who are currently intubated;
  • Patients who recently (< 6months) had an MI or stroke;
  • Pregnant woman; There will be no exclusion based on gender, race or ethnicity.

结局指标

主要结局

Reduction in anatomical dead space and improvement in ventilatory efficiency

时间窗: 30 minutes

次要结局

  • Improvement of ventilation rate, tidal volume, end tidal CO2, arterial pH, PaCO2, and PaO2, SpO2, pulse rate, blood pressure and patient rating of comfort of each ventilatory pattern.(30 minutes)

研究者

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

Yandong Jiang

Assistant Professor of Anesthesia

Massachusetts General Hospital

研究点 (2)

Loading locations...

相似试验