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Post Intubation Laryngeal Hazards in Children in the Pediatric Intensive Care Unit

Post Intubation Laryngeal Hazards in Children in the Pediatric Intensive Care Unit

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06198634
Enrollment
30
Registered
2024-01-10
Start date
2024-01-15
Completion date
2026-01-01
Last updated
2024-01-10

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Laryngeal Injury

Brief summary

this study aims to detect the effect of endotracheal intubation on the larynx of the pediatric population in order to allow early detection of any hazards

Detailed description

Laryngeal lesions in children can be caused by a number of risk factors, including patient variables (prematurity, cardiac comorbidities), intubation method (in an emergency, by an unskilled team), and endotracheal tube use. (large size, cuffed tube), longer duration of intubation, infection, and insufficient patient sedation are just a few risk factors that can contribute to the development of laryngeal lesions in children. Endoscopic imaging of the larynx is essential in pediatric intubation-related laryngeal injuries since the intensity of symptoms may not necessarily be correlated with the extent of laryngeal injury that is actually present. Therefore, after intubation, we will evaluate neonates, babies, and kids who have laryngeal problems. The flexible fiberoptic nasopharyngo-laryngoscope, or laryngoscopy, is the preferred technique to assess these children's issues and represents a substantial development in the diagnosis of laryngeal pathology in children. As well as rigid bronchoscopy and direct laryngoscopy, under general anesthesia. The risks associated with anesthesia and instrumentation are two key drawbacks of this method. Without transferring to the operating room or requiring general anesthesia, the infant can be assessed in the outpatient clinic. Direct observation of the nasopharynx and larynx in a professional environment

Interventions

None listed

Sponsors

Assiut University
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
2 Months to 18 Years
Healthy volunteers
No

Inclusion criteria

1. Age: from 2 month to 18 year 2. Gender: both sexes will be included in the study 3. Endotracheal intubation in emergency or elective sitting for 24hr or more

Exclusion criteria

* 1-Congenital laryngeal lesions 2-Head and neck surgery 3-CNS infections 4-Craniofacial malformations

Design outcomes

Primary

MeasureTime frameDescription
measurement of pediatric post intubation laryngeal lesions7_10 days post_intubationmeasurement of presence or absence of laryngeal lesions (supraglottic,glottic,subglottic) post intubation in pediatrics using fiberoptic naso\_pharyngeal\_laryngoscopy

Contacts

Primary ContactAshrakt Ahmed, master
ashrkt1710@gmail.com01111709156

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026