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临床试验/NCT06698120
NCT06698120尚未招募不适用

Assessment of Efficacy and Safety of Awake Prone Positioning in Sickle Cell Anemia Patient Admitted in Intensive Care Unit for Severe Acute Chest Syndrome

Assistance Publique - Hôpitaux de Paris2 个研究点 分布在 1 个国家目标入组 15 人开始时间: 2026年1月1日最近更新:
适应症

试验速览

阶段
不适用
状态
尚未招募
入组人数
15
试验地点
2
主要终点
The total duration of APP during the stay in intensive care unit

研究概览

简要总结

Acute chest syndrome (ACS) is the leading cause of admission to intensive care and the leading cause of death in patients with sickle cell disease. Irrespective of the cause of ACS, there is an heterogeneity in pulmonary ventilation/perfusion ratios, leading to worsening of the disease.

Efficiency of awake prone positioning (APP) in acute respiratory failure (ARF) was particularly highlighted during the COVID-19 pandemic. Several physiological factors contribute to this benefit including an improvement in ventilatory drive and gas exchange.

The investigator hypothesize that APP could lead to clinical improvement in ACS in terms of oxygenation and ventilatory drive, by improving the heterogeneity of ventilation

详细描述

  • Several physiological mechanisms contribute to the benefit of APP during ARF. In addition to hypoxemia improvement, there is also an effect on ventilatory drive, notably in terms of polypnea, ROX index and inspiratory effort.
  • Considering that hypoxemia in ACS contributes to the physiopathological process: deoxygenation of haemoglobin S - red blood cells falciformisation - vaso-occlusive event, APP could be an additional therapy in severe ACS. In addition, improving ventilation-perfusion ratios, mainly by recruiting dorsal zones, could be particularly useful in ACS, where pulmonary damage predominates in gravito-dependent zones.

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

  • Age >18 years
  • Major sickle cell anemia (SS, SC, Sβ)
  • Admission in intensive care unit for ACS
  • Registered in the French social insurance regime.
  • Written, informed consent

排除标准

  • Pregnant or breastfeeding women
  • Immediate need for intubation
  • Impaired vigilance status (Glasgow scale score < 12)
  • Pneumothorax
  • Haemodynamically unstable
  • Thoracic trauma admission
  • Severely obese with body-mass index higher than 40 kg/m²
  • EIT contraindication: pacemaker, automatic implantable defibrillators, skin lesions facing the EIT belt, unstable rachis fracture or medullary lesions

结局指标

主要结局

The total duration of APP during the stay in intensive care unit

时间窗: 28 days

次要结局

  • GI measured by EIT(Up to 28 days)
  • ΔEELI measured by EIT(Up to 28 days)
  • Changes in respiratory parameters(Up to 28 days)
  • Pain measurement assessed by visual analog scale,(Up to 28 days)
  • Pain measurement assessed by morphine consumption(Up to 28 days)
  • Pain measurement assessed by analgesic therapeutic escalation(Up to 28 days)
  • Occurrence of skin lesions during the intensive care unit stay(28 Days)
  • Occurrence of displacement of devices during the intensive care unit stay(28 Days)
  • Occurrence of use of vital support therapy during the intensive care unit stay(28 Days)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (2)

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