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Randomized Trial Investigating Four Nasal CPAP Systems in the Management of Apnea of Prematurity

NCT00482040 · Status: TERMINATED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 16

Last updated 2007-08-24

No results posted yet for this study

Summary

The purpose of this study is to evaluate four different nasal continuous pressure systems, which are usually applied on our neonatal intensive care unit, with regard of their effect on bradycardia and desaturations in preterm infants.

Conditions

  • Continuous Positive Airway Pressure
  • Apnea of Prematurity
  • CPAP

Interventions

DEVICE

Stephanie (TM), Infant Flow (TM), Infant Flow advance (TM), Bubble CPAP

Sponsors & Collaborators

  • University Hospital Tuebingen

    lead OTHER

Principal Investigators

  • Tobias Pantalitschka, MD · University children´s hospital Tuebingen

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
SINGLE
Model
CROSSOVER

Eligibility

Max Age
14 Weeks
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2004-03-31
Completion
2006-01-31

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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 NCT00482040 on ClinicalTrials.gov