MedTrace Logo

Non-invasive Secondary Respiratory Support in Late Preterm and Term Infants

NCT07000071 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 40

Last updated 2025-05-31

No results posted yet for this study

Summary

The aim of the present work is to compare between various modes of non-invasive respiratory support (including NCPAP, NIPPV, and NHFOV) as secondary respiratory support modes in late preterm and term neonates as regards the need for reintubation. Additionally, the study aims at comparing between the three modes concerning the associated morbidity and mortality.

Conditions

  • Neonates
  • Respiratory Distress
  • Non- Invasive Ventilation

Interventions

DEVICE

NCPAP

Apply nasal continuous positive airway pressure in intubated patients with respiratory distress at time of weaning

DEVICE

NIPPV

Apply nasal intermittent positive pressure ventilation in intubated patients with respiratory distress at time of weaning

DEVICE

NHFOV

Apply nasal high frequency ventilation in intubated patients with respiratory distress at time of weaning

Sponsors & Collaborators

  • Alexandria University

    lead OTHER

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
1 Day
Max Age
14 Days
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2021-07-01
Primary Completion
2021-12-30
Completion
2022-01-30

Countries

  • Egypt

Study Locations

More Related Trials

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07000071 on ClinicalTrials.gov