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By Assessing the Continuous Respiratory Physiological Changes Through Prone Position, Determine the Optimal Duration for Prone Position

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National Taiwan University

Status

Enrolling

Conditions

Prone Position
Electrical Impedance Tomography
Acute Respiratory Distress Syndrome

Treatments

Device: Electrical Impedance Tomography

Study type

Observational

Funder types

Other

Identifiers

NCT06827184
202310137DIND

Details and patient eligibility

About

The prone position leads to a more homogeneous distribution of ventilation by inflation of collapsed alveoli and reduction in alveolar hyperinflation. By employing EIT, the study can obtain a thorough comprehension of the ongoing alterations in regional ventilation before and after adopting the prone position. It is also anticipated that there is an impact on inflammation biomarkers before and after the prone position. This assessment aids in determining the ideal duration for prone position therapy, encompassing the necessary hours and days in the prone position.

Full description

The prone position leads to a more homogeneous distribution of ventilation by inflation of collapsed alveoli and reduction in alveolar hyperinflation. By employing EIT, the study can obtain a thorough comprehension of the ongoing alterations in regional ventilation before and after adopting the prone position. It is also anticipated that there is an impact on inflammation biomarkers before and after the prone position. This assessment aids in determining the ideal duration for prone position therapy, encompassing the necessary hours and days in the prone position.

Therefore, the investigators propose a project with the aim of collecting relevant clinical, laboratory, imaging, and respiratory physiology data from consenting patients with ARDS within the study period. The objective is to analyze changes in biomarkers following prone position.

Enrollment

100 estimated patients

Sex

All

Ages

18+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  1. Acute respiratory distress syndrome
  2. Age > 18
  3. Serial arterial blood gas data:PaO2/FiO2 <150. The mechanical ventilator setting:FiO2>0.6, PEEP>5 cmH2O

Exclusion criteria

  1. Implantable electronic devices (e.g., pacemakers)
  2. Body mass index > 30
  3. Major thoracic and abdominal surgery
  4. Patients with unstable spine and pelvis conditions
  5. Pregnant women in the second and third trimesters
  6. Patients with head trauma, elevated intracranial pressure, or elevated intraocular pressure
  7. Hemodynamically unstable patients unsuitable for prone ventilation therapy
  8. Patients with active seizures

Trial contacts and locations

1

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Central trial contact

Ting-Yu Liao, MD

Data sourced from clinicaltrials.gov

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