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
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
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
NCT ID
NCT00482040
First Posted
June 1, 2007
Last Updated
August 23, 2007
Sponsor
University Hospital Tuebingen
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
Learn more about this trial
Randomized Trial Investigating Four Nasal CPAP Systems in the Management of Apnea of Prematurity
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