Pilot Study of Topical Steroid for Prevention of Chronic Lung Disease in Extremely Premature Infants.
Primary Purpose
Bronchopulmonary Dysplasia
Status
Unknown status
Phase
Phase 2
Locations
United States
Study Type
Interventional
Intervention
Infasurf
Pulmicort
Sham
Sponsored by
About this trial
This is an interventional prevention trial for Bronchopulmonary Dysplasia focused on measuring Bronchopulmonary Dysplasia, Budesonide, Infasurf
Eligibility Criteria
Inclusion Criteria:
- Birth weight 501-1000 g and ≤ 28 weeks gestational age
- Diagnosed as RDS requiring mechanical ventilation and surfactant therapy during the first 4 hours after birth
- Still ventilated on day 5-9 of life.
- An interval of at least 24 hours' duration between the last dose of indomethacin and the endotracheal instillation of study drug.
Exclusion Criteria:
- Congenital or chromosomal anomalies
- Occurrence of perinatal sepsis
- Use of intravenous steroids > 7 days
Sites / Locations
- NICU-Pitt County Memorial HospitalRecruiting
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Experimental
Active Comparator
Sham Comparator
Arm Label
A (two study drugs group)
B (one study drug group)
C (no study drug group)
Arm Description
The standard management + two study drugs (endotracheal instillation of a mixture containing budesonide and Infasurf)
The standard management + one study drug (endotracheal instillation of Infasurf only).
The standard management only.
Outcomes
Primary Outcome Measures
To measure the effect of surfactant with and without Budesonide on the development of BPD in ELBW infants.
The main goal of the study is to determine whether endotracheal instillation of surfactant (Infasurf) with or without potent topical steroid (Budesonide) reduces the development of Bronchopulmonary Dysplasia (BPD) in Extremely Low Birth Weight (ELBW) infants at high risk of BPD.
Secondary Outcome Measures
To measure the effect of surfactant with and without Budesonide on the inflammatory cytokines in tracheal aspirates.
Tracheal aspirate samples will be collected before instillation of each dose of the study drug, 7 days after the last dose if the infant is still intubated, and prior to elective extubation regardless of when extubation occurs. Tracheal aspirate samples will be obtained from the control (standard management) group in the same way and using the same time frame as the treatment groups
Full Information
NCT ID
NCT01268215
First Posted
December 28, 2010
Last Updated
December 28, 2010
Sponsor
East Carolina University
1. Study Identification
Unique Protocol Identification Number
NCT01268215
Brief Title
Pilot Study of Topical Steroid for Prevention of Chronic Lung Disease in Extremely Premature Infants.
Official Title
The Effect of Endotracheal Instillation of Surfactant With and Without Budesonide on the Development of Bronchopulmonary Dysplasia in Ventilator-dependent, Extremely Low Birth Weight Infants: A Pilot Study
Study Type
Interventional
2. Study Status
Record Verification Date
July 2010
Overall Recruitment Status
Unknown status
Study Start Date
July 2010 (undefined)
Primary Completion Date
June 2012 (Anticipated)
Study Completion Date
December 2013 (Anticipated)
3. Sponsor/Collaborators
Name of the Sponsor
East Carolina University
4. Oversight
Data Monitoring Committee
Yes
5. Study Description
Brief Summary
A Pilot study to evaluate the safety and the efficacy of endotracheal instillation of pulmonary surfactant, with or without topical steroid (Budesonide), as a prophylactic treatment for Bronchopulmonary Dysplasia (a form of chronic lung disease) in extremely low birth weight infants. Cytokines (a group of inflammatory mediators) are measured in the tracheal aspirate before and after instillation of the study drugs.
Detailed Description
Bronchopulmonary Dysplasia (BPD) is still one of the most common complications of ventilated premature infants. Lung inflammation plays a major role in its pathogenesis. Systemic steroids can be given to control this inflammatory process but their widespread use is limited by their systemic side effects and concerns for long neurodevelopmental adverse sequelae. Delivering steroids by inhalation which has been proven to be effective in young infants with asthma has been shown to be unsatisfactory for ELBW infants with BPD. This may be due to the fact that current delivery devices do not meet the requirements of the specific anatomical and physiologic characteristics of the airways and breathing patterns in this special group of patients. A novel approach to facilitate delivery directly to the lungs, thereby avoiding systemic concerns has been demonstrated in a recent study in which budesonide ( a topical steroid) was given to ventilated preterm infants using surfactant as a vehicle.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Bronchopulmonary Dysplasia
Keywords
Bronchopulmonary Dysplasia, Budesonide, Infasurf
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Parallel Assignment
Masking
ParticipantCare ProviderInvestigatorOutcomes Assessor
Allocation
Randomized
Enrollment
45 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
A (two study drugs group)
Arm Type
Experimental
Arm Description
The standard management + two study drugs (endotracheal instillation of a mixture containing budesonide and Infasurf)
Arm Title
B (one study drug group)
Arm Type
Active Comparator
Arm Description
The standard management + one study drug (endotracheal instillation of Infasurf only).
Arm Title
C (no study drug group)
Arm Type
Sham Comparator
Arm Description
The standard management only.
Intervention Type
Drug
Intervention Name(s)
Infasurf
Other Intervention Name(s)
Calfactant
Intervention Description
Endotracheal instillation of Infasurf once per week for three weeks
Intervention Type
Drug
Intervention Name(s)
Pulmicort
Other Intervention Name(s)
Budesonide
Intervention Description
Endotracheal instillation, once per week for three weeks
Intervention Type
Other
Intervention Name(s)
Sham
Other Intervention Name(s)
Air Sham
Intervention Description
None instilled through the endotracheal tube
Primary Outcome Measure Information:
Title
To measure the effect of surfactant with and without Budesonide on the development of BPD in ELBW infants.
Description
The main goal of the study is to determine whether endotracheal instillation of surfactant (Infasurf) with or without potent topical steroid (Budesonide) reduces the development of Bronchopulmonary Dysplasia (BPD) in Extremely Low Birth Weight (ELBW) infants at high risk of BPD.
Time Frame
Supplemental oxygen requirement at 36 weeks' postmenstrual age (PMA)
Secondary Outcome Measure Information:
Title
To measure the effect of surfactant with and without Budesonide on the inflammatory cytokines in tracheal aspirates.
Description
Tracheal aspirate samples will be collected before instillation of each dose of the study drug, 7 days after the last dose if the infant is still intubated, and prior to elective extubation regardless of when extubation occurs. Tracheal aspirate samples will be obtained from the control (standard management) group in the same way and using the same time frame as the treatment groups
Time Frame
The measurement of cytokines in tracheal aspirate samples will be done at the end of the study.
10. Eligibility
Sex
All
Minimum Age & Unit of Time
24 Weeks
Maximum Age & Unit of Time
28 Weeks
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Birth weight 501-1000 g and ≤ 28 weeks gestational age
Diagnosed as RDS requiring mechanical ventilation and surfactant therapy during the first 4 hours after birth
Still ventilated on day 5-9 of life.
An interval of at least 24 hours' duration between the last dose of indomethacin and the endotracheal instillation of study drug.
Exclusion Criteria:
Congenital or chromosomal anomalies
Occurrence of perinatal sepsis
Use of intravenous steroids > 7 days
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Waleed Maamoun, MD
Phone
1-252-744-3945
Email
maamounw@ecu.edu
First Name & Middle Initial & Last Name or Official Title & Degree
James Cummings, MD
Phone
1-252-744-4787
Email
CummingsJ@ecu.edu
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Waleed M Maamoun, MD
Organizational Affiliation
Pitt County Memorial Hospital/Brody School of Medicine at East Carolina University
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
James Cummings, MD
Organizational Affiliation
Pitt County Memorial Hospital/Brody School of Medicine at East Carolina University
Official's Role
Study Director
First Name & Middle Initial & Last Name & Degree
Scott MacGilvray, MD
Organizational Affiliation
Pitt County Memorial Hospital/Brody School of Medicine at East Carolina University
Official's Role
Study Chair
First Name & Middle Initial & Last Name & Degree
Karl Kaminski, RRT-NPS
Organizational Affiliation
Pitt County Memorial Hospital/Brody School of Medicine at East Carolina University
Official's Role
Study Chair
Facility Information:
Facility Name
NICU-Pitt County Memorial Hospital
City
Greenville
State/Province
North Carolina
ZIP/Postal Code
27834
Country
United States
Individual Site Status
Recruiting
12. IPD Sharing Statement
Learn more about this trial
Pilot Study of Topical Steroid for Prevention of Chronic Lung Disease in Extremely Premature Infants.
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