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临床试验/NCT01104610
NCT01104610撤回不适用

Target Volume With a Pressure Controlled Ventilator in Obesity Hypoventilation Syndrome With Persistent Oxygen Desaturations With Continuous Positive Airway Pressure

Breas Medical S.A.R.L.3 个研究点 分布在 1 个国家开始时间: 2009年5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
撤回
发起方
试验地点
3
主要终点
Evolution of daytime PaCO2 of NIV without target volume, with Target volume and with CPAP alone

研究概览

简要总结

The purpose of this study is to investigate the evolution of daytime partial pressure of carbon dioxide in the blood (PaCO2) after 6 weeks of noninvasive ventilation-pressure support ventilation (NIV-PSV) with target volume versus continuous positive airway pressure (CPAP) alone versus NIV-PSV.

详细描述

Compare the efficacy between 3 ventilation modes (CPAP, PSV and PSV with Target Volume) on patients with obesity hypoventilation syndrome already treated with CPAP but with persistent desaturations.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Parallel
主要目的
Supportive Care
盲法
Triple (Participant, Care Provider, Investigator)

入排标准

年龄范围
20 Years 至 75 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients from 20 to 75 years old.
  • Body mass index > 32 kg/m2
  • Nocturnal oxygen desaturation 5 mn ≤ 88% under CPAP,
  • PaCO2 > 5,9 kPa in diurnal, spontaneous ventilation

排除标准

  • Patients with COPD and VEMS/FVC < 65%
  • Patients with CHF and periodic breathing (Ejection Fraction <40%)
  • Patients with a recent respiratory decompensation in the month preceding inclusion

研究组 & 干预措施

NIV-PSV without Target Volume

Active Comparator

Pressure Support Non Invasive Ventilation without Target Volume

干预措施: Breas Vivo 40 (Device)

NIV-PSV with Target Volume

Active Comparator

Non Invasive Pressure Support Ventilation with Target Volume set

干预措施: Breas Vivo 40 (Device)

NIV-CPAP

Active Comparator

Pressure Support Ventilation in CPAP mode

干预措施: Breas Vivo 40 (Device)

结局指标

主要结局

Evolution of daytime PaCO2 of NIV without target volume, with Target volume and with CPAP alone

时间窗: 6 weeks

次要结局

  • Evolution of subjective and objective sleepness (Osler)(6 weeks)
  • Evolution of quality of ventilation (Leaks, asynchronism, others events)(6 weeks)
  • Evolution of blood inflammation (IL6, TNFα et CRP)(6 weeks)
  • Evolution in dyspnea scores (BDI/TDI and Simon Score)(6 weeks)
  • Compliance (hours of treatment)(6 weeks)
  • Cardiovascular parameters on Arterial strength (pulse velocity) and Endothelial function (Post ischemic test)(6 weeks)
  • Evolution of insulin résistance(6 weeks)
  • Sleep quality (PSG) between the 3 groups at 6 weeks(6 weeks)

研究者

发起方
Breas Medical S.A.R.L.
申办方类型
Industry
责任方
Sponsor

研究点 (3)

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