Actively Recruiting

Age: 16Years +
All Genders
NCT06192342

Ventilatory Parameters in Acute Neurological Injury

Led by Ramos Mejía Hospital · Updated on 2026-03-30

19

Participants Needed

1

Research Sites

160 weeks

Total Duration

On this page

AI-Summary

What this Trial Is About

The goal of this observational study is to test the association between baseline ventilatory parameters (in particular mechanical power (MP), mechanical power normalized to predicted body weight (MP/PBW) and driving pressure (DP) with the baseline neurological status (assessed through the Glasgow coma score) in adults patients under mechanical ventilation with acute neurological injury secondary to stroke, brain trauma or subarachnoid hemorrhage. The main question\[s\]it aims to answer are: 1. In patients with acute neurological injury under mechanical ventilation, is there a correlation between the acute neurological injury, assessed using the Glasgow scale on admission, and baseline ventilatory parameters? 2. In patients with acute neurological injury under mechanical ventilation, are the baseline ventilatory parameters altered at baseline?

CONDITIONS

Official Title

Ventilatory Parameters in Acute Neurological Injury

Who Can Participate

Age: 16Years +
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Acute neurological injury in patients 16 years of age or older
  • Requiring mechanical ventilation for neurological causes
  • No baseline lung injury, defined as normal chest x-ray and adequate oxygenation
  • PaO2/FiO2 ratio of 300 or greater
  • Use of Neumovent TS and Neumovent Advance respirators
Not Eligible

You will not qualify if you...

  • Pneumothorax or presence of a pleural drainage tube
  • Hemodynamic instability with mean blood pressure 65 mmHg or lower
  • Use of high doses of inotropes (Norepinephrine greater than 0.5 gammas/kilo/minute or equivalent)
  • PaO2/FiO2 ratio less than 80 mmHg
  • Chronic obstructive pulmonary disease (COPD)
  • Pregnancy

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 1 location

1

Roberto Santa Cruz

Ciudad Autonoma de Buenos Aires, Buenos Aires, Argentina, B6600KCL

Actively Recruiting

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Research Team

R

Roberto S Santa Cruz, Dr.

CONTACT

A

Antonella Civile, Dr.

CONTACT

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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