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Early CPAP in Respiratory Distress Syndrome

NCT00368680 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 256

Last updated 2010-12-24

No results posted yet for this study

Summary

The purpose of this study is to establish if a strategy of EBCPAP application in a subgroup of VLBWI, 800 to 1500g birthweight, decreases the need for mechanical ventilation in this group, without affecting mortality.

Conditions

  • Respiratory Distress Syndrome

Interventions

DEVICE

Early Bubble CPAP

Sponsors & Collaborators

  • Pontificia Universidad Catolica de Chile

    lead OTHER

Principal Investigators

  • José Luis Tapia, MD · Pontificia Universidad Católica

  • Aldo Bancalari, MD · Hospital Guillermo Grant

  • Soledad Urzua, MD · Pontificia Universidad Católica

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
5 Minutes
Max Age
30 Minutes
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2007-01-31
Primary Completion
2008-04-30
Completion
2009-09-30

Countries

  • Argentina
  • Chile
  • Paraguay
  • Peru
  • Uruguay

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 NCT00368680 on ClinicalTrials.gov