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Clinical Trials/NCT05527431
NCT05527431
Completed
N/A

High Flow Nasal Cannula vs Noninvasive Ventilation in Patients With Hypoxic Respiratory Failure Following Blunt Chest Trauma, a Randomized Clinical Trial

Ain Shams University1 site in 1 country120 target enrollmentAugust 1, 2022

Overview

Phase
N/A
Intervention
Not specified
Conditions
Blunt Injury of Thorax
Sponsor
Ain Shams University
Enrollment
120
Locations
1
Primary Endpoint
PaO2/FiO2 ratio
Status
Completed
Last Updated
last year

Overview

Brief Summary

to compare high flow nasal cannula against noninvasive ventilation in patients with non-sever blunt chest trauma in improvement of oxygenation, need for intubation and mechanical ventilation within 28 days

Registry
clinicaltrials.gov
Start Date
August 1, 2022
End Date
April 1, 2024
Last Updated
last year
Study Type
Interventional
Study Design
Parallel
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Age ≥18 y,
  • Willing and able to provide written informed consent prior to performing study procedures,
  • currently hospitalized and requiring medical care for non-sever blunt chest trauma (abbreviated injury severity scale ≤ 2) SpO2 90% or less while breathing 10 L/min.

Exclusion Criteria

  • Contraindications of noninvasive ventilation (face trauma or surgery, airway obstruction, upper gastrointestinal tract bleeding, disturbed level of consciousness), -smoker
  • intubation for any cause other than respiratory cause

Outcomes

Primary Outcomes

PaO2/FiO2 ratio

Time Frame: 3 successive days

mean value of three successive PaO2/FiO2 ratio in mmHg between both groups

Secondary Outcomes

  • Discomfort score(3 successive days)

Study Sites (1)

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