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Clinical Trials/NCT05509088
NCT05509088UnknownNot Applicable

Impact of the Early Use of High Flow Nasal Cannula in Patients With Post-traumatic Lung Contusion, a Randomized Clinical Trial

Ain Shams University2 sites in 1 country120 target enrollmentStarted: July 28, 2022Last updated:
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Conditions

Trial Snapshot

Phase
Not Applicable
Enrollment
120
Locations
2
Primary Endpoint
need for intubation and mechanical ventilation within 28 days of randomization.
Study OverviewStudy DesignEligibility CriteriaOutcomesInvestigatorsSitesRecords & IdentifiersSimilar Trials

Study Overview

Brief Summary

We hypothesize that early and continuous administration of oxygen via high flow nasal cannula in patients with lung contusion and non-severe acute lung injury might reduce the incidence of intubation and hold the deterioration of pulmonary functions.

Study Design

Study Type
Interventional
Allocation
Randomized
Intervention Model
Parallel
Primary Purpose
Prevention
Masking
None

Eligibility Criteria

Ages
18 Years to 80 Years (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • •Willing and able to provide written informed consent prior to performing study procedures, currently hospitalized and requiring medical care for blunt chest trauma, within 24h of trauma

Exclusion Criteria

  • •face trauma or surgery, airway obstruction, known to have chronic chest condition

Outcomes

Primary Outcomes

need for intubation and mechanical ventilation within 28 days of randomization.

Time Frame: 3 months

the incidence of intubation in patients with lung contusion who receive oxygen through high flow nasal cannula

Secondary Outcomes

No secondary outcomes reported

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (2)

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Impact of the Early Use of High Flow Nasal... | Clinical Trial