Actively Recruiting

Age: 18Years +
All Genders
ID05150483

EndotyPIng PreHospitAl de Novo Acute hYpoxemic Respiratory Failure

Led by Evangelismos Hospital · Updated on 2025-08-07

250

Participants Needed

1

Research Sites

5 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

Researchers are studying critically ill adults who arrive at the emergency department with new acute hypoxemic respiratory failure (AHRF), a severe condition affecting lung oxygen levels. The study aims to identify different biological subtypes, or endotypes, of AHRF by analyzing changes in blood proteins over 24 hours. It also seeks to find which early clinical, imaging, physiological, and biological factors relate to patient outcomes like death or ongoing severe low oxygen. Participants are adults with AHRF needing at least 5 liters per minute of oxygen to keep oxygen saturation at 90% or higher and who are newly experiencing this condition without previous long-term oxygen use. The study collects two blood samples 24 hours apart to track biomarker changes and builds models to predict risks of death or persistent severe hypoxemia. It also creates a protein panel to improve outcome prediction. The study organizes a registry and biobank of these patients for research. During the study, researchers collect clinical data, radiological images, physiological measures, and biological samples soon after emergency department presentation. They follow participants for up to 28 days or until hospital discharge or death, tracking outcomes like mortality, days free from intensive care, ventilators, or other supports, and infection occurrences. The main measure is identifying dynamic AHRF endotypes through blood protein patterns. This observational study involves no treatment but detailed monitoring and data collection to understand AHRF better.

CONDITIONS

Brief Title

EndotyPIng PreHospitAl de Novo Acute hYpoxemic Respiratory Failure

Who Can Participate

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Adult patients (aged >18 years) presenting in the emergency department
  • De novo acute hypoxemic respiratory failure requiring oxygen flow rate of 5 liters per minute or more to maintain SpO2 of 90% or more
Not Eligible

You will not qualify if you...

  • Age <18 years
  • Not admitted to the hospital
  • Postoperative acute respiratory failure within one week from surgery
  • Chronic hypoxemic respiratory failure requiring long term oxygen therapy at home
  • Hypercapnic respiratory failure
  • Transferred from another hospital or facility
  • Pregnant women
  • Admitted to the hospital purely to facilitate comfort care
  • Lack of informed consent

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Monitoring

Duration - Up to 28 days following presentation to the emergency department

Participants presenting with de novo acute hypoxemic respiratory failure are observed with collection of clinical, radiological, physiological, and biological data including two blood samples taken 24 hours apart to identify disease endotypes and predict outcomes.

Assessments during hospital stay until discharge or death

Trial Site Locations

Total: 1 location

1

Evangelismos Hospital

Athens, Attica, Greece, 10676

Actively Recruiting

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Research Team

E

Eleni D. Papoutsi, MD

How is the study designed?

Study Type

OBSERVATIONAL

Masking

N/A

Allocation

N/A

Model

N/A

Primary Purpose

N/A

Number of Arms

1

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Published Research Related To This Trial

Acute respiratory distress syndrome without identifiable risk factors: A secondary analysis of the ARDS network trials.

John S Harrington, Edward J Schenck, Clara Oromendia...

https://pubmed.ncbi.nlm.nih.gov/29898428

Effect of Neutropenic Critical Illness on Development and Prognosis of Acute Respiratory Distress Syndrome.

David R Price, Katherine L Hoffman, Clara Oromendia...

https://pubmed.ncbi.nlm.nih.gov/32986956