Nasal Intermittent Positive Pressure Ventilation in Premature Infants (NIPPV) (NIPPV)
Primary Purpose
Respiratory Insufficiency of Prematurity
Status
Completed
Phase
Phase 3
Locations
International
Study Type
Interventional
Intervention
nCPAP
NIPPV
Sponsored by
About this trial
This is an interventional prevention trial for Respiratory Insufficiency of Prematurity focused on measuring prematurity, respiratory insufficiency, non-invasive ventilation, bronchopulmonary dysplasia, hyaline membrane disease
Eligibility Criteria
Inclusion Criteria:
- Birth weight <1000 gm
- Gestational age <30 completed weeks
Intention to manage the infant with non-invasive respiratory support (i.e. no endotracheal tube), where either:
- the infant is within the first 7 days of life and has never been intubated or has received less than 24 hours of total cumulative intubated respiratory support;
- the infant is within the first 28 days of life, has been managed with intubated respiratory support for 24 hours or more and is a candidate for extubation followed by non-invasive respiratory support.
Exclusion Criteria:
- Considered non-viable by clinician (decision not to administer effective therapies)
- Life-threatening congenital abnormalities including congenital heart disease (excluding patent ductus arteriosis)
- Infants known to require surgical treatment
- Abnormalities of the upper and lower airways
- Neuromuscular disorders
- Infants who are >28 days old and continue to require mechanical ventilation with an endotracheal tube
Sites / Locations
- Georgetown University Children's Medical Center
- The George Washington University Hospital
- Tufts University Medical Center
- Beth Israel Deaconess Medical Center (BIDMC)
- Virtua West Jersey Hospital
- SUNY Downstate Medical Center
- Kings County Hospital
- New York Hospital Queens
- Queens Hospital Center
- Brookdale University Hospital & Medical Center
- Stony Brook University Medical Center
- Pennsylvania Hospital/U. of Pennsylvania
- Children's Hospital of Philadelphia
- University of Utah
- LKH Feldkirch
- CHC St. Vincent
- St. Boniface General Hospital/University of Manitoba
- Winnipeg Health Sciences Centre
- IWK Health Centre
- McMaster University
- Children's Hospital of Eastern Ontario
- The Ottawa Hospital General Campus
- Hospital for Sick Children
- Royal University Hospital
- Cork University Maternity Hospital
- Coombe Women's Hospital
- National Maternity Hospital
- University Medical Center Groningen/Beatrix Children's Hosp
- Princess Amalia Dept of Pediatrics, Isala Clinics
- Hamad Medical Corporation
- KK Women's and Children's Hospital
- Karolinska University Hospital/Astrid Lingrenn's Children's Hospital
- Royal Maternity Hospital
- University of Leicester
- St. Mary's Hospital
Arms of the Study
Arm 1
Arm 2
Arm Type
Active Comparator
Active Comparator
Arm Label
A
B
Arm Description
Non-invasive respiratory support via nasal intermittent positive pressure ventilation
Non-invasive respiratory support via nasal Continuous Positive Airway Pressure
Outcomes
Primary Outcome Measures
Composite of survival to 36 weeks gestational age, free of moderate-severe bronchopulmonary dysplasia
Secondary Outcome Measures
All cause mortality at 36 weeks gestational age
All cause mortality before first discharge home
retinopathy of prematurity
ultrasonographic evidence of brain injury
necrotizing enterocolitis
growth
time to establish full feeds
nosocomial infections
need for re-intubation
time on supplemental oxygen
duration of positive pressure respiratory support
comparison of synchronized and non-synchronized NIPPV
bronchopulmonary dysplasia
air leak syndromes
nasal trauma
Full Information
NCT ID
NCT00433212
First Posted
February 7, 2007
Last Updated
December 3, 2014
Sponsor
McMaster University
Collaborators
Canadian Institutes of Health Research (CIHR)
1. Study Identification
Unique Protocol Identification Number
NCT00433212
Brief Title
Nasal Intermittent Positive Pressure Ventilation in Premature Infants (NIPPV)
Acronym
NIPPV
Official Title
Efficacy and Safety of NIPPV to Increase Survival Without Bronchopulmonary Dysplasia in Extremely Low Birth Weight Infants
Study Type
Interventional
2. Study Status
Record Verification Date
December 2014
Overall Recruitment Status
Completed
Study Start Date
April 2007 (undefined)
Primary Completion Date
August 2011 (Actual)
Study Completion Date
December 2011 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
McMaster University
Collaborators
Canadian Institutes of Health Research (CIHR)
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
The machines and oxygen used to help very premature babies breathe can have side-effects, such as bronchopulmonary dysplasia (BPD). Infants with BPD get more complications (a higher death rate, a longer time in intensive care and on assisted ventilation, more hospital readmissions in the first year of life, and more learning problems) than infants who do not develop BPD. Doctors try to remove the tube in the wind-pipe that links the baby to the breathing machine as soon as possible. However, small babies get tired, and still require help to breathe. One of the standard and common techniques to help them breathe without a tube in the wind-pipe is to use simple pressure support, nasal continuous positive airway pressure or nCPAP. This supports breathing a little, but it is often not enough to prevent the need to go back on the breathing machine.
Nasal intermittent positive pressure ventilation (NIPPV) is similar to nCPAP, but also gives some breaths, or extra support, to babies through a small tube in the nose. NIPPV is safe and effective, and already in use as an alternate "standard" therapy.
The main research question: After being weaned from the breathing machine, is NIPPV better than nCPAP in preventing BPD in premature babies weighing 999 grams or less at birth?
Detailed Description
The immature lung of extremely low birth weight (ELBW, < 1000 g) infants is easily damaged by the placement of an endotracheal tube to deliver mechanical ventilation and oxygen. This and the total time of mechanical ventilation contributes to bronchopulmonary dysplasia (BPD). Infants with BPD have an increased risk of later death or neuro-impairment. With the increasing survival of ELBW infants in the NICU, there has been a proportionate increase in the number of infants surviving with BPD.
Following invasive ventilation via an endotracheal tube (ETT), extubation to nasal Continuous Positive Airway Pressure (nCPAP)ventilation is the standard approach. Currently, 40% of infants who are extubated and given nCPAP support fail, and require re-intubation. Previous work suggests that a less invasive respiratory support such as Nasal Intermittent Positive Pressure Ventilation (NIPPV), without an endotracheal tube is less injurious to the lung. NIPPV may thereby reduce the duration of invasive ventilator support, and aid successful early extubation. We hypothesize that the use of NIPPV leads to a higher rate of survival without BPD than standard therapy with nCPAP.
This randomized clinical trial is appropriately powered to compare NIPPV with nCPAP to detect effects on clinically relevant long-term outcomes, such as death and BPD at 36 weeks. This is a multi-national, randomized, open clinical trial of two different standard methods of providing non-invasive respiratory support to 1000 extremely preterm infants weighing less than 1000 grams at birth.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Respiratory Insufficiency of Prematurity
Keywords
prematurity, respiratory insufficiency, non-invasive ventilation, bronchopulmonary dysplasia, hyaline membrane disease
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
1011 (Actual)
8. Arms, Groups, and Interventions
Arm Title
A
Arm Type
Active Comparator
Arm Description
Non-invasive respiratory support via nasal intermittent positive pressure ventilation
Arm Title
B
Arm Type
Active Comparator
Arm Description
Non-invasive respiratory support via nasal Continuous Positive Airway Pressure
Intervention Type
Device
Intervention Name(s)
nCPAP
Intervention Description
Deliver non-invasive respiratory support via ventilator with nCPAP device
Intervention Type
Device
Intervention Name(s)
NIPPV
Intervention Description
Deliver non-invasive respiratory support via ventilator with NIPPV device
Primary Outcome Measure Information:
Title
Composite of survival to 36 weeks gestational age, free of moderate-severe bronchopulmonary dysplasia
Time Frame
36 weeks gestational age
Secondary Outcome Measure Information:
Title
All cause mortality at 36 weeks gestational age
Time Frame
36 weeks gestational age
Title
All cause mortality before first discharge home
Time Frame
first discharge home
Title
retinopathy of prematurity
Time Frame
discharge home
Title
ultrasonographic evidence of brain injury
Time Frame
36 weeks gestional age
Title
necrotizing enterocolitis
Time Frame
36 weeks gestational age
Title
growth
Time Frame
discharge home
Title
time to establish full feeds
Time Frame
discharge home
Title
nosocomial infections
Time Frame
discharge home
Title
need for re-intubation
Time Frame
36 weeks gestational age
Title
time on supplemental oxygen
Time Frame
discharge home
Title
duration of positive pressure respiratory support
Time Frame
discharge home
Title
comparison of synchronized and non-synchronized NIPPV
Time Frame
discharge home
Title
bronchopulmonary dysplasia
Time Frame
36 weeks gestational age
Title
air leak syndromes
Time Frame
36 weeks gestational age
Title
nasal trauma
Time Frame
discharge home
10. Eligibility
Sex
All
Maximum Age & Unit of Time
28 Days
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Birth weight <1000 gm
Gestational age <30 completed weeks
Intention to manage the infant with non-invasive respiratory support (i.e. no endotracheal tube), where either:
the infant is within the first 7 days of life and has never been intubated or has received less than 24 hours of total cumulative intubated respiratory support;
the infant is within the first 28 days of life, has been managed with intubated respiratory support for 24 hours or more and is a candidate for extubation followed by non-invasive respiratory support.
Exclusion Criteria:
Considered non-viable by clinician (decision not to administer effective therapies)
Life-threatening congenital abnormalities including congenital heart disease (excluding patent ductus arteriosis)
Infants known to require surgical treatment
Abnormalities of the upper and lower airways
Neuromuscular disorders
Infants who are >28 days old and continue to require mechanical ventilation with an endotracheal tube
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Haresh Kirpalani, MD, MSc
Organizational Affiliation
Hamilton Health Sciences Corporation
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Brigitte Lemyre, MD
Organizational Affiliation
Children's Hospital of Eastern Ontario
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Aaron Chiu, MD
Organizational Affiliation
St. Boniface Hospital
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
David Millar, MD
Organizational Affiliation
Royal Maternity Hospital, Belfast
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Robin S Roberts, MTech
Organizational Affiliation
Hamilton Health Sciences/McMaster University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Bradley Yoder, MD
Organizational Affiliation
University of Utah
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Peter H Dijk, MD, PhD
Organizational Affiliation
University Medical Centrum Groningen
Official's Role
Study Director
Facility Information:
Facility Name
Georgetown University Children's Medical Center
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20007
Country
United States
Facility Name
The George Washington University Hospital
City
Washington
State/Province
District of Columbia
ZIP/Postal Code
20037
Country
United States
Facility Name
Tufts University Medical Center
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02111
Country
United States
Facility Name
Beth Israel Deaconess Medical Center (BIDMC)
City
Boston
State/Province
Massachusetts
ZIP/Postal Code
02215
Country
United States
Facility Name
Virtua West Jersey Hospital
City
Voorhees
State/Province
New Jersey
ZIP/Postal Code
08043
Country
United States
Facility Name
SUNY Downstate Medical Center
City
Brooklyn
State/Province
New York
ZIP/Postal Code
11023
Country
United States
Facility Name
Kings County Hospital
City
Brooklyn
State/Province
New York
ZIP/Postal Code
11203
Country
United States
Facility Name
New York Hospital Queens
City
Brooklyn
State/Province
New York
ZIP/Postal Code
11355
Country
United States
Facility Name
Queens Hospital Center
City
Jamaica
State/Province
New York
ZIP/Postal Code
11432
Country
United States
Facility Name
Brookdale University Hospital & Medical Center
City
New York
State/Province
New York
ZIP/Postal Code
11212
Country
United States
Facility Name
Stony Brook University Medical Center
City
Stony Brook
State/Province
New York
ZIP/Postal Code
11794-8111
Country
United States
Facility Name
Pennsylvania Hospital/U. of Pennsylvania
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19035
Country
United States
Facility Name
Children's Hospital of Philadelphia
City
Philadelphia
State/Province
Pennsylvania
ZIP/Postal Code
19104
Country
United States
Facility Name
University of Utah
City
Salt Lake City
State/Province
Utah
ZIP/Postal Code
84158-1289
Country
United States
Facility Name
LKH Feldkirch
City
Feldkirch
ZIP/Postal Code
6800
Country
Austria
Facility Name
CHC St. Vincent
City
Rocourt
ZIP/Postal Code
B-4000
Country
Belgium
Facility Name
St. Boniface General Hospital/University of Manitoba
City
Winnipeg
State/Province
Manitoba
ZIP/Postal Code
R3E 0L8
Country
Canada
Facility Name
Winnipeg Health Sciences Centre
City
Winnipeg
State/Province
Manitoba
Country
Canada
Facility Name
IWK Health Centre
City
Halifax
State/Province
Nova Scotia
Country
Canada
Facility Name
McMaster University
City
Hamilton
State/Province
Ontario
ZIP/Postal Code
L8S 4J9
Country
Canada
Facility Name
Children's Hospital of Eastern Ontario
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8L1
Country
Canada
Facility Name
The Ottawa Hospital General Campus
City
Ottawa
State/Province
Ontario
ZIP/Postal Code
K1H 8L6
Country
Canada
Facility Name
Hospital for Sick Children
City
Toronto
State/Province
Ontario
Country
Canada
Facility Name
Royal University Hospital
City
Saskatoon
State/Province
Saskatchewan
Country
Canada
Facility Name
Cork University Maternity Hospital
City
Wilton
State/Province
Cork
Country
Ireland
Facility Name
Coombe Women's Hospital
City
Dublin
Country
Ireland
Facility Name
National Maternity Hospital
City
Dublin
Country
Ireland
Facility Name
University Medical Center Groningen/Beatrix Children's Hosp
City
Groningen
ZIP/Postal Code
9700 RB
Country
Netherlands
Facility Name
Princess Amalia Dept of Pediatrics, Isala Clinics
City
Zwolle
ZIP/Postal Code
8000 GK
Country
Netherlands
Facility Name
Hamad Medical Corporation
City
Doha
Country
Qatar
Facility Name
KK Women's and Children's Hospital
City
Singapore
ZIP/Postal Code
229899
Country
Singapore
Facility Name
Karolinska University Hospital/Astrid Lingrenn's Children's Hospital
City
Stockholm
ZIP/Postal Code
S-171 76
Country
Sweden
Facility Name
Royal Maternity Hospital
City
Belfast
State/Province
Northern Ireland
ZIP/Postal Code
BT12 6BB
Country
United Kingdom
Facility Name
University of Leicester
City
Leicester
ZIP/Postal Code
LE1 6TP
Country
United Kingdom
Facility Name
St. Mary's Hospital
City
London
ZIP/Postal Code
W2 1NY
Country
United Kingdom
12. IPD Sharing Statement
Citations:
PubMed Identifier
23944299
Citation
Kirpalani H, Millar D, Lemyre B, Yoder BA, Chiu A, Roberts RS; NIPPV Study Group. A trial comparing noninvasive ventilation strategies in preterm infants. N Engl J Med. 2013 Aug 15;369(7):611-20. doi: 10.1056/NEJMoa1214533.
Results Reference
result
PubMed Identifier
29275926
Citation
Bamat NA, Guevara JP, Bryan M, Roberts RS, Yoder BA, Lemyre B, Chiu A, Millar D, Kirpalani H. Variation in Positive End-Expiratory Pressure Levels for Mechanically Ventilated Extremely Low Birth Weight Infants. J Pediatr. 2018 Mar;194:28-33.e5. doi: 10.1016/j.jpeds.2017.10.065. Epub 2017 Dec 22.
Results Reference
derived
PubMed Identifier
26162889
Citation
Millar D, Lemyre B, Kirpalani H, Chiu A, Yoder BA, Roberts RS. A comparison of bilevel and ventilator-delivered non-invasive respiratory support. Arch Dis Child Fetal Neonatal Ed. 2016 Jan;101(1):F21-5. doi: 10.1136/archdischild-2014-308123. Epub 2015 Jul 10.
Results Reference
derived
Learn more about this trial
Nasal Intermittent Positive Pressure Ventilation in Premature Infants (NIPPV)
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