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Two Strategies of RDS Treatment in Newborns With Birth Weight > 1500 Grams

NCT00277030 · Status: UNKNOWN · Phase: PHASE4 · Type: INTERVENTIONAL · Enrollment: 110

Last updated 2006-08-24

No results posted yet for this study

Summary

The purpose of this study is to compare two different treatment strategies for RDS in preterm infants \> 1500 grams and evaluate whether a selective surfactant administration would reduce the need of intubation, mechanical ventilation and surfactant use.

Conditions

  • Respiratory Distress Syndrome

Interventions

DRUG

Surfactant

DEVICE

Nasal CPAP

Sponsors & Collaborators

  • Sociedad Chilena de Pediatría

    collaborator UNKNOWN

  • Pontificia Universidad Catolica de Chile

    lead OTHER

Principal Investigators

  • Soledad Urzua, MD · Pontificia Universidad Católica

  • Alvaro Gonzalez, MD · Pontificia Universidad Católica

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
5 Minutes
Max Age
1 Day
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2006-01-31

Countries

  • Chile

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 NCT00277030 on ClinicalTrials.gov