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

Primary Purpose

Continuous Positive Airway Pressure, Apnea of Prematurity, CPAP

Status
Terminated
Phase
Not Applicable
Locations
Study Type
Interventional
Intervention
Stephanie (TM), Infant Flow (TM), Infant Flow advance (TM), Bubble CPAP
Sponsored by
University Hospital Tuebingen
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Continuous Positive Airway Pressure focused on measuring CPAP, Preterm, Prematurity, Apnea of prematurity

Eligibility Criteria

undefined - 14 Weeks (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • gestational age at birth < 34 weeks
  • postconceptional age and body weight at study ≤38 week and >1000 g
  • requirement for N-CPAP to treat AOP as judged by the attending neonatologist

Exclusion Criteria:

  • congenital or chromosomal abnormalities
  • acute infections
  • intraventricular hemorrhage
  • additional inspired oxygen to maintain pulse oximeter saturation SpO2 >92%
  • patent ductus arteriosus

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Cumulative percentage of bradycardia (heart rate <80 beats/min) and desaturation (SaO2 <80%) per hour

    Secondary Outcome Measures

    - Event rates for central apneas, desaturations and bradycardias calculated as the number of respective events per hour of artefact free recording time - relative cumulative event time - baseline heart rate, respiratory rate and oxygen saturation

    Full Information

    First Posted
    June 1, 2007
    Last Updated
    August 23, 2007
    Sponsor
    University Hospital Tuebingen
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00482040
    Brief Title
    Randomized Trial Investigating Four Nasal CPAP Systems in the Management of Apnea of Prematurity
    Official Title
    Randomized Trial Investigating Four Nasal CPAP Systems in the Management of Apnea of Prematurity
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    May 2007
    Overall Recruitment Status
    Terminated
    Why Stopped
    Recruiting took longer than expected due to a lack of eligible patients (very strong inclusion and exclusion criterias)
    Study Start Date
    March 2004 (undefined)
    Primary Completion Date
    undefined (undefined)
    Study Completion Date
    January 2006 (Actual)

    3. Sponsor/Collaborators

    Name of the Sponsor
    University Hospital Tuebingen

    4. Oversight

    Data Monitoring Committee
    No

    5. Study Description

    Brief 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.
    Detailed Description
    BACKGROUND: Apnea of prematurity (AOP) is a common problem in preterm infants. Nasal respiratory support using either Continuous Positive Airway Pressure (CPAP) or Intermittent Mandatory Ventilation (IMV) are, among others, widely used treatments. Which of the different systems is the most efficient, however, is unclear. OBJECTIVE: Efficiency of different CPAP systems on reducing the cumulative percentage of bradycardia and desaturation in preterm infants. METHODS: In a prospective, randomized, cross-over trial 32 preterm infants Infants will randomly allocated to receive nasal CPAP delivered by one of the following sys-tems: (1) a conventional IMV-System (Stephanie, Stephan GmbH, Germany with PIP 15 cmH2O, RR 10/min) delivering CPAP via short binasal prongs (Hudson RCI, USA); (2) the Infant-Flow-System (EME Ltd, Great Britain) with CPAP delivery via short binasal prongs; (3) the Infant-Flow-AdvanceTM-System used in the pressure assist mode with PIP 10 cmH2O, RR 10/min; and (4) a nasal underwater bubble CPAP with application via binasal prongs (Hudson RCI, USA). All systems will be adjusted to achieve an approximate PEEP of 6 cm H2O. Each study lasts 24 hours, during which chest wall and abdominal movements, SaO2, tcPCO2, ECG, esopha-gus pressure and CPAP-/IMV-pressure will be recorded continuously. Infants will be studied in room air in a 15° head tilt prone position while being treated with caffeine (3mg/kg/d). PRIMARY OUTCOME MEASURE Cumulative percentage of bradycardia (heart rate <80/min) and desaturation (SaO2 <80%) per hour.

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Continuous Positive Airway Pressure, Apnea of Prematurity, CPAP
    Keywords
    CPAP, Preterm, Prematurity, Apnea of prematurity

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Not Applicable
    Interventional Study Model
    Crossover Assignment
    Masking
    Single
    Allocation
    Randomized
    Enrollment
    16 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Device
    Intervention Name(s)
    Stephanie (TM), Infant Flow (TM), Infant Flow advance (TM), Bubble CPAP
    Primary Outcome Measure Information:
    Title
    Cumulative percentage of bradycardia (heart rate <80 beats/min) and desaturation (SaO2 <80%) per hour
    Time Frame
    one year
    Secondary Outcome Measure Information:
    Title
    - Event rates for central apneas, desaturations and bradycardias calculated as the number of respective events per hour of artefact free recording time - relative cumulative event time - baseline heart rate, respiratory rate and oxygen saturation
    Time Frame
    one year

    10. Eligibility

    Sex
    All
    Maximum Age & Unit of Time
    14 Weeks
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: gestational age at birth < 34 weeks postconceptional age and body weight at study ≤38 week and >1000 g requirement for N-CPAP to treat AOP as judged by the attending neonatologist Exclusion Criteria: congenital or chromosomal abnormalities acute infections intraventricular hemorrhage additional inspired oxygen to maintain pulse oximeter saturation SpO2 >92% patent ductus arteriosus
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Tobias Pantalitschka, MD
    Organizational Affiliation
    University children´s hospital Tuebingen
    Official's Role
    Principal Investigator

    12. IPD Sharing Statement

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

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