跳至主要内容
临床试验/NCT07823296
NCT07823296尚未招募不适用

Assessment of Blood Viscosity in ARDS

Hospices Civils de Lyon1 个研究点 分布在 1 个国家目标入组 46 人开始时间: 2026年10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
尚未招募
入组人数
46
试验地点
1
主要终点
Comparison of Blood Viscosity in Patients with ARDS and Control Group on Day 1

研究概览

简要总结

Acute respiratory distress syndrome (ARDS) is characterized by damage to the alveolar-capillary membrane, resulting in hypoxemia, decreased pulmonary compliance, and hemodynamic changes.

Critical conditions (hypoxia; septic shock associated with ARDS) can alter blood viscosity. These changes in viscosity can affect blood flow and hemodynamics.

There is only one clinical study that has measured one of the determinants of blood viscosity in ARDS (deformability), even though other parameters are involved in viscosity (elongation, deformability, hematocrit, etc.), and it is possible to measure blood viscosity comprehensively. To date, therefore, no study has evaluated the various parameters of blood viscosity in ARDS.

The aim of this study is to investigate hyperviscosity in patients with ARDS and to assess whether this hyperviscosity correlates with respiratory or hemodynamic changes.

The investigators will therefore compare blood viscosity and its determinants in patients admitted to the intensive care unit for ARDS and in patients admitted for other reasons (excluding ARDS or sepsis/septic shock).

The investigators will also conduct a longitudinal assessment of changes in hemodynamic, respiratory, and viscosity parameters during ARDS

研究设计

研究类型
Observational
观察模型
Case Control
时间视角
Prospective

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

  • Inclusion Criteria:
  • Age ≥ 18 ans
  • Moderate-to-severe ARDS according to the global definition:
  • with PaO₂/FiO₂ ≤ 200 mmHg (based on arterial blood gas analysis in patients receiving invasive or non-invasive mechanical ventilation or high-flow nasal oxygen therapy).
  • Participation agreement obtained (either from the patient themselves or from a relative)

排除标准

  • ARDS that has been present for more than 72 hours
  • Terminally ill patient with death expected within 24 hours
  • Patient who has received a blood transfusion within the past month
  • Patient with a known hematologic malignancy (lymphoma; myeloma; acute or chronic leukemia)
  • Patient with a known hemoglobinopathy.
  • Hemorrhagic shock
  • Hemoglobin < 70 g/dL
  • Control group
  • Inclusion Criteria:
  • Age ≥ 18 ans
  • Participation agreement obtained (either from the patient themselves or from a relative)
  • Exclusion Criteria:
  • Presence of ARDS according to the global definition
  • P/F < 300 mmHg
  • Presence of sepsis defined by an infection and a SOFA score delta ≥
  • Terminally ill patient with death expected within 24 hours
  • Patient who has received a blood transfusion within the past month
  • Patient with a known hematologic malignancy (lymphoma; myeloma; acute or chronic leukemia)
  • Patient with a known hemoglobinopathy.
  • Hemorrhagic shock
  • Hemoglobin < 70 g/dL

研究组 & 干预措施

Case group

Patients over 18 years of age with moderate to severe ARDS (overall definition) (P/F <200)

干预措施: Blood draws (peripheral venous puncture) (Biological)

Case group

Patients over 18 years of age with moderate to severe ARDS (overall definition) (P/F <200)

干预措施: Blood draws (arterial catheter, central venous line, or Swan-Ganz catheter) (Other)

Control group

Patients admitted to intensive care unit without ARDS or sepsis/septic shock

干预措施: Blood draws (peripheral venous puncture) (Biological)

结局指标

主要结局

Comparison of Blood Viscosity in Patients with ARDS and Control Group on Day 1

时间窗: At day 1

Blood viscosity will be determined after complete oxygenation of the blood, at native hematocrit, at a temperature of 25 °C. Measurements will be performed at different shear rates (11.5, 22.5, 45, 90, and 225 s-¹) using a cone-plate viscometer (Brookfield DVII+ equipped with a CPE40 cone, Brookfield Engineering Labs, Natick, MA, USA). This technique is based on applying a well-defined shear rate gradient between a moving conical surface and a fixed flat surface, with the blood sample placed between them. The fluid subjected to this shear resists flow in proportion to its viscosity. The higher the viscosity, the greater the torque required to maintain motion. This approach allows for the precise measurement of the apparent viscosity of blood across a wide range of mechanical stresses, replicating the flow conditions encountered in the bloodstream. The value at 225 s-¹ will be used as the primary endpoint (with an accuracy of 5-10 centipoise at this shear rate).

次要结局

未报告次要终点

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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