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UnknownNCT03206489

Nasal High Frequency Oscillation for Respiratory Distress Syndrome in Twins Infants

Nasal High Frequency Oscillation for Respiratory Distress Syndrome in Preterm Twins Infants

Status
Unknown
Phase
N/A
Study type
Interventional
Enrollment
200 (estimated)
Sponsor
Daping Hospital and the Research Institute of Surgery of the Third Military Medical University · Academic / Other
Sex
All
Age
30 Minutes – 6 Hours
Healthy volunteers
Not accepted

Summary

The investigators compared advantages and disadvantages of two forms of noninvasive respiratory support -noninvasive high-frequency oscillatory ventilation (nHFOV) or nasal continuous positive airway pressure (nCPAP) -as a primary mode of ventilation in preterm twins infants with respiratory distress syndrome

Detailed description

Invasive ventilation is related to development of adverse pulmonary and nonpulmonary outcomes in ventilated infants. Various modes of noninvasive respiratory support are being increasingly used to minimize the incidence of bronchopulmonary dysplasia (BPD). The aim of this trial to compare the effects of noninvasive high frequency oscillatory ventilation (NHFOV) and nasal continuous positive airway pressure (NCPAP) in preterm twins infants as the primary mode.

Conditions

Interventions

TypeNameDescription
DEVICEnoninvasive high-frequency ventilation (nHFOV)noninvasive high-frequency ventilation (nHFOV) as a primary mode of ventilation in one of the preterm twins infants with respiratory distress syndrome
DEVICEnasal continuous positive airway pressure (nCPAP)nasal continuous positive airway pressure (nCPAP) as a primary mode of ventilation in another of the preterm twins infants with respiratory distress syndrome

Timeline

Start date
2017-08-01
Primary completion
2024-06-30
Completion
2024-06-30
First posted
2017-07-02
Last updated
2022-10-25

Locations

1 site across 1 country: China

Source: ClinicalTrials.gov record NCT03206489. Inclusion in this directory is not an endorsement.