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NOT YET RECRUITING
NCT07823296

Assessment of Blood Viscosity in ARDS (Acute Respiratory Distress Syndrome)

Sponsor: Hospices Civils de Lyon

View on ClinicalTrials.gov

Summary

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

Official title: Assessment of Blood Viscosity in ARDS

Key Details

Gender

All

Age Range

18 Years - Any

Study Type

OBSERVATIONAL

Enrollment

46

Start Date

2026-10-01

Completion Date

2028-01-01

Last Updated

2026-09-16

Healthy Volunteers

No

Conditions

Interventions

BIOLOGICAL

Blood draws (peripheral venous puncture)

Procedure performed by intensive care nurses. Case group : Daily blood draws (4 mL) for 7 days. Control group : blood draws (4 mL) on Day 1.

OTHER

Blood draws (arterial catheter, central venous line, or Swan-Ganz catheter)

Case group : For patients with an arterial catheter, central venous line, or Swan-Ganz catheter, an additional blood sample will be collected on Day 1.

Locations (1)

Hopital de la Croix-Rousse

Lyon, France