Health TrialsbyHealthPanel

Is High Resolution Endotracheal Tube Leak Data Indicative of the Development of Post-extubation Stridor in Children?

ConditionPost Extubation Stridor
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 16
SponsorUniversity Hospital, Antwerp

About this trial

Post extubation stridor (PES) is a common and possibly serious complication of invasive ventilation via endotracheal tube (ETT) in pediatric intensive care (PICU) patients. The source of the PES is either temporary in the case of post-intubation laryngeal edema, or long-term in the case of subglottic stenosis.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age 0 - 16 years

Ventilation via endotracheal tube for at least 6 hours

Disqualifiers

None

Trial population

All ventilated children under 16 years will be eligible for thus study

Trial design

Design model

Cohort

Time perspective

Retrospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Post-Extubation Stridor

(PES, definition = requirement of nebulized adrenaline)

Time frame
during ICU admission

Secondary outcomes

1

Reintubation

Need for reintubation

Time frame
during ICU admission
2

Diagnostic procedure

Need for diagnostic procedure

Time frame
during ICU admission
3

Surgical airway

Need for surgical airway

Time frame
during ICU admission

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

University Hospital, Antwerp

Lead sponsor

Source ClinicalTrials.gov
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