Comparison of Two Methods of Continuous Positive Airway Pressure (CPAP) to Support Successful Extubation of Infants of Birth Weights ≤ 1500 Grams (C2CPAP)
Primary Purpose
Premature Birth, Respiratory Insufficiency
Status
Unknown status
Phase
Not Applicable
Locations
Canada
Study Type
Interventional
Intervention
Infant Flow System
Bubble CPAP
Sponsored by
About this trial
This is an interventional treatment trial for Premature Birth focused on measuring premature infant, supporting extubation
Eligibility Criteria
Inclusion Criteria: Intubated infant ≤ 1500 grams at birth Decision to extubate to CPAP made by the clinical team Written informed consent obtained Exclusion Criteria: Have known airway anomalies Have grade III or IV or periventricular leukomalacia Have known or suspected genetic syndromes
Sites / Locations
- Sunnybrook & Women's College Health Sciences CentreRecruiting
Outcomes
Primary Outcome Measures
failure of extubation as defined by the following: pH < 7.25 and PCO2 > 65 (or an increase of 15 mmHg from pre-extubation), a sustained (> 1 hour) increase in FiO2 of .15 (as compared to pre-extubation) or significant apno
Secondary Outcome Measures
reintubation
length of time in days on CPAP
corrected gestational age at cessation of CPAP
average weight gain on CPAP
assessment of pain will
Full Information
NCT ID
NCT00187434
First Posted
September 14, 2005
Last Updated
January 22, 2007
Sponsor
Sunnybrook Health Sciences Centre
Collaborators
Ontario Lung Association
1. Study Identification
Unique Protocol Identification Number
NCT00187434
Brief Title
Comparison of Two Methods of Continuous Positive Airway Pressure (CPAP) to Support Successful Extubation of Infants of Birth Weights ≤ 1500 Grams (C2CPAP)
Official Title
A Randomized Control Trial Comparing Two Methods of Delivering Continuous Positive Airway Pressure (CPAP), Infant Flow System CPAP and Bubble CPAP, in Supporting Successful Extubation of Infants of Birth Weights Less Than or Equal to 1500 Grams at Birth (C2CPAP)
Study Type
Interventional
2. Study Status
Record Verification Date
September 2005
Overall Recruitment Status
Unknown status
Study Start Date
September 2003 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
undefined (undefined)
3. Sponsor/Collaborators
Name of the Sponsor
Sunnybrook Health Sciences Centre
Collaborators
Ontario Lung Association
4. Oversight
5. Study Description
Brief Summary
Continuous positive airway pressure (CPAP) has been used successfully to promote extubation in the premature infant population. The two methods of CPAP to be examined are currently used by many institutions, yet no study has compared these methods to determine which is better in the population of newborns < 1500 grams (birth weight) at supporting extubation. This randomised controlled study will examine two types of CPAP: the Infant Flow System and the Bubble CPAP. This randomised controlled, single site, clinical study is to determine whether the Bubble CPAP or the Infant Flow System (IFS) CPAP is more effective at supporting the extubation in infants of birth weights < 1500 grams. Seventy-six infants will be randomised, immediately prior to extubation, to IFS or Bubble CPAP of 5 cmH2O. The primary outcome is successful extubation, defined as not reaching failure criteria for the 7 days post-extubation. Failure criteria are defined as pH < 7.25 and PCO2 > 65 mmHg or a sustained increase in FiO2 of 0.15.
Detailed Description
Background: Continuous Positive Airway Pressure (CPAP) has been used successfully to promote extubation in the premature infant population (Davis & Henderson-Smart, 2002). The two methods of CPAP to be examined are used by many institutions, yet no study has compared these methods to determine which is better in the population of newborns < 1500 grams (birth weight) at supporting extubation. This study may have cost savings implications. If bubble CPAP is shown to be as effective in this application neonatal intensive care units (NICUs) will have a more affordable option of providing effective CPAP.
Methods: This randomised controlled, single site, clinical study is to determine if Bubble CPAP or Infant Flow System (IFS) CPAP is more effective at supporting extubation in infants of birth weights < 1500 grams. Seventy-six infants will be randomised immediately prior to extubation to IFS or Bubble CPAP of 5 cmH2O. The primary outcome is successful extubation, defined as not reaching failure criteria for the 7 days post-extubation. Failure criteria are defined as pH < 7.25 and PCO2 > 65 mmHg or a sustained increase in FiO2 of 0.15.
Participants: Parents/guardians of eligible infants will be approached and given information regarding the study, and any questions answered. They will then be allowed to consider study participation in private. The recruiter will return at an agreed time and informed consent will be obtained from those agreeing to participate. Parents will be approached in accordance with the guidelines of the NICU @ SWCHSC. Infants are eligible if birth weight < 1500 grams, are to be extubated to CPAP and have no known airway anomalies, or suspected genetic anomalies.
Analysis: Multiple ANOVA analysis will be used for continuous variables, chi-square for categorical variables, including primary outcome.
Conclusion: The results of this study will determine which method of CPAP is the best method of supporting extubation in the < 1500 g infant.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Premature Birth, Respiratory Insufficiency
Keywords
premature infant, supporting extubation
7. Study Design
Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
76 (false)
8. Arms, Groups, and Interventions
Intervention Type
Device
Intervention Name(s)
Infant Flow System
Intervention Type
Device
Intervention Name(s)
Bubble CPAP
Primary Outcome Measure Information:
Title
failure of extubation as defined by the following: pH < 7.25 and PCO2 > 65 (or an increase of 15 mmHg from pre-extubation), a sustained (> 1 hour) increase in FiO2 of .15 (as compared to pre-extubation) or significant apno
Secondary Outcome Measure Information:
Title
reintubation
Title
length of time in days on CPAP
Title
corrected gestational age at cessation of CPAP
Title
average weight gain on CPAP
Title
assessment of pain will
10. Eligibility
Sex
All
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Intubated infant
≤ 1500 grams at birth
Decision to extubate to CPAP made by the clinical team
Written informed consent obtained
Exclusion Criteria:
Have known airway anomalies
Have grade III or IV or periventricular leukomalacia
Have known or suspected genetic syndromes
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Marilyn D Hyndman
Phone
416 323 6400
Ext
4172
Email
marilyn.hyndman@sw.ca
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Marilyn D Hyndman
Organizational Affiliation
Sunnybrook & Women's College Health Sciences Centre
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sunnybrook & Women's College Health Sciences Centre
City
Toronto
State/Province
Ontario
ZIP/Postal Code
M4L 2Y6
Country
Canada
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Marilyn D Hyndman
Phone
416 323 6400
Ext
4172
Email
marilyn.hyndman@sw.ca
First Name & Middle Initial & Last Name & Degree
Marilyn D Hyndman
12. IPD Sharing Statement
Learn more about this trial
Comparison of Two Methods of Continuous Positive Airway Pressure (CPAP) to Support Successful Extubation of Infants of Birth Weights ≤ 1500 Grams (C2CPAP)
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