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Nasal Intermittent Positive-Pressure Ventilation for Twin Infants With Respiratory Distress Syndrome

NCT01926106 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 286

Last updated 2017-12-07

No results posted yet for this study

Summary

In the present study, we hypothesized that primary mode nIPPV initiated shortly after birth would decrease the incidence of intubation or death in twin infants when compared to nCPAP.

Conditions

  • Neonatal Respiratory Distress Syndrome

Interventions

DEVICE

nIPPV

one of the twins was randomly allocated to nIPPV

DEVICE

nCPAP

another of the twins was allocated to nCPAP

Sponsors & Collaborators

  • Daping Hospital and the Research Institute of Surgery of the Third Military Medical University

    lead OTHER

Principal Investigators

  • Long Chen, MD · Department of Pediatrics, Daping Hospital, Research Institute of Surgery, Third Military Medical University,

Study Design

Allocation
RANDOMIZED
Purpose
SUPPORTIVE_CARE
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
30 Minutes
Max Age
6 Hours
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2012-07-01
Primary Completion
2017-07-30
Completion
2017-07-30

Countries

  • China

Study Locations

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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 NCT01926106 on ClinicalTrials.gov