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NCT07414472: PES

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

Recruiting now Last updated 17 February 2026
What this trial tests

trial in Post Extubation Stridor in 400 participants. Currently enrolling.

Timeline
30 June 2025
Primary endpoint
30 June 2026
30 June 2026

Quick facts

Lead sponsorUniversity Hospital, Antwerp
StatusRecruiting now
Study typeOBSERVATIONAL
Enrollment400
Start date30 June 2025
Primary completion30 June 2026
Estimated completion30 June 2026
Sites1 location across Belgium

Conditions studied

Sponsor

University Hospital, Antwerp

Who can join

Under 16, any sex, with Post Extubation Stridor. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

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.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other University Hospital, Antwerp trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT07414472.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing