Predictors of Prolonged Mechanical Ventilation in Preterm Infants

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
AgeUp to 36
SponsorAssiut University

About this trial

This prospective cohort study aims to identify the independent predictors of prolonged mechanical ventilation in preterm infants admitted to the Neonatal Intensive Care Unit of Assiut University Children Hospital.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

- Preterm infants born before 37 completed weeks of gestation

Admission to the NICU within the neonatal period

Requirement for invasive mechanical ventilation

Written informed consent from parents or legal guardians

Disqualifiers

- Infants born after 37 weeks of gestation

Major congenital anomalies

Chromosomal abnormalities

Congenital neuromuscular disorders

Trial population

Preterm infants admitted to the Neonatal Intensive Care Unit of Assiut University Children Hospital who require invasive mechanical ventilation.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

100 Participants
are grouped into 2 trial groups
Group A: Prolonged Mechanical Ventilation
Group B: Non-Prolonged Mechanical Ventilation

Trial outcomes

Primary outcomes

1

Occurrence of prolonged mechanical ventilation

Proportion of preterm infants who require invasive mechanical ventilation for more than 7 days or frequent reintubation.

Time frame
Up to 30 days

Secondary outcomes

1

Duration of invasive mechanical ventilation

Total number of days of invasive mechanical ventilation.

Time frame
Up to 30 days
2

Successful extubation rate

Proportion of infants who are successfully extubated without re-intubation within 48-72 hours.

Time frame
Up to 30 days
3

Incidence of bronchopulmonary dysplasia

Proportion of infants diagnosed with bronchopulmonary dysplasia.

Time frame
Up to 30 days
4

Incidence of neonatal sepsis

Proportion of infants diagnosed with neonatal sepsis.

Time frame
Up to 30 days

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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