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临床试验/NCT04363463
NCT04363463已完成不适用

Impact of Prone Position in Patients Under Spontaneous Breathing on Intubation or Non-invasive Ventilation or Death Incidence During COVID-19 Acute Respiratory Distress

Centre Hospitalier Régional d'Orléans34 个研究点 分布在 2 个国家目标入组 268 人开始时间: 2020年8月28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
268
试验地点
34
主要终点
Percent age of patients who will have endotracheal intubation or non-invasive ventilation at two pressure levels and/or die, in each of the 2 randomization groups.

研究概览

简要总结

The SARS-Cov2 viral pandemic is responsible for a new infectious disease called COVID-19 (CoronaVIrus Disease), is a major health problem. Respiratory complications occur in 15 to 40%, the most serious is acute respiratory distress syndrome (ARDS).

The management of COVID-19 is essentially symptomatic with respiratory oxygen supplementation in mild forms to invasive mechanical ventilation in the most severe forms.

Prone position (PP) reduced mortality in patients with ARDS in intensive care. Ding et al showed that PP and high flow oxygenation reduced the intubation in patients with moderate to severe ARDS.

The investigators hypothesize that the use of PP in spontaneously ventilation patients under oxygen standard could decrease incidence of intubation or non-invasive ventilation or death compared to conventional positioning management in medical departments.

详细描述

This is a multicenter randomized controlled study. 400 patients with COVID-19 documentation and undergoing oxygen therapy will be randomly assigned, with a 1:1 ratio, to conventional positioning or repeated prone sessions.

The control group will have conventional positioning: semi-seated in bed or seated in a chair. The prone position is not allowed during the day (it is allowed at night if it is the natural sleeping position).

The intervention group will have:

  • Two sessions minimum of prone position over the day. With a total objective of at least 2h30 of cumulated duration over the day. The objective is to spend as much time as possible in prone position if the patient tolerates it well.
  • The maximum of prone position at night. Patients must be able to take position by themselves or with minimal assistance. The rails will be positioned in order to prevent falling out of bed. The patient will be free to choose his preferred prone position as long as the back is not compressed

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
None

入排标准

年龄范围
18 Years 至 85 Years(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Patients aged from 18 to 85 years old
  • With COVID-19 documentation
  • Undergoing oxygen therapy (nasal cannula, medium or high concentration mask or high flow nasal oxygen therapy)
  • Able to move to PP by him/herself or with minimal assistance
  • Written consent
  • Hospitalized in COVID medical department for less than 72 hours

排除标准

  • Pregnant (positive pregnancy test during screening) or breastfeeding women
  • Patient on long-term oxygen therapy or Continuous Positive Airway Pressure (CPAP) or Non-Invasive Ventilation (NIV) at home
  • Chronic Obstructive Pulmonary Disease (COPD) Patient stage 3 or 4
  • Patient with known chronic diffuse interstitial lung disease
  • Patient with neuromuscular pathology
  • Contraindication to the PP (recent thoracic trauma, pneumothorax, orthopaedic fracture preventing mobilization, ...)
  • Deep vein thrombosis of the lower limbs or pulmonary embolism with effective anticoagulation for less than 48 hours
  • Hemodynamic instability (MAP < 65 mm Hg) persisting for more than 1 hour
  • Respiratory rate greater than 40 cycles per minute
  • Excessive use of accessory respiratory muscles (as judged by the clinician)
  • Indication for curative NIV (acute pulmonary edema or acute hypercapnic respiratory failure)
  • Intestinal Occlusive Syndrome
  • Patient unable to protect upper airway
  • Inability to understand French or to follow instructions for the prone position.
  • Person under guardianship
  • Protected Majors
  • Not affiliated to French social security
  • Decision not to forgo life sustaining therapy
  • Patient discharged from an intensive care unit and has been treated by invasive or non-invasive mechanical ventilation at 2 pressure levels during the resuscitation stay.

结局指标

主要结局

Percent age of patients who will have endotracheal intubation or non-invasive ventilation at two pressure levels and/or die, in each of the 2 randomization groups.

时间窗: Day 28

To show that PP in spontaneously ventilation patients could reduce the risk of acquiring the following event (composite endpoint): * Endotracheal intubation * Or non-invasive ventilation (NIV) with two pressure levels * And/or death

次要结局

  • Rate (%) of need for transfer to intensive care unit(Day 28)
  • Duration in days for the change of 2 points on the WHO ordinal scale(Day 28)
  • Rate (%) of non-invasive ventilation at two pressure levels in the 2 randomization groups(Day 28)
  • Duration of oxygen therapy in the 2 randomization groups.(Day 28)
  • Hospital mortality and mortality at D28 in the 2 randomization groups(Day 28)
  • Rate (%) of intubation and invasive ventilation in the 2 randomization groups.(Day 28)
  • Duration of hospitalization in the 2 randomization groups.(Day 28)
  • Rate (%) of use of non-invasive ventilation at two pressure levels, intubation throughout the entire stay when the stay is longer than 28 days.(1 year)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (34)

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