Lung DiseasesNCT00005293
Antecedents of Bronchopulmonary Dysplasia
An observational study of Lung Diseases and Bronchopulmonary Dysplasia, run by National Heart, Lung, and Blood Institute (NHLBI).
Trial summary
To identify risk factors for bronchopulmonary dysplasia/chronic pulmonary disease of prematurity and to estimate proportions of this group of disorders attributable to antenatal risk factors, perinatal events, and neonatal care procedures. Read more about this study
- Who is it for?
- Ages Up to 100 years, men only
- Conditions the study is for
- Lung Diseases, Bronchopulmonary Dysplasia
- How many people
- Not given
- Where
- No sites listed yet
- Study dates
- Dec 1988to Nov 1990
- Phase
- Observational
- Are there results?
- None posted in the registry
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages Up to 100 years
- Men only
- No healthy volunteers
- Child, Adult, Older adult
No eligibility criteria
About this study
To identify risk factors for bronchopulmonary dysplasia/chronic pulmonary disease of prematurity and to estimate proportions of this group of disorders attributable to antenatal risk factors, perinatal events, and neonatal care procedures.
Read the detailed description
BACKGROUND:
The Phenobarbital Prophylaxis for Neonatal Intracranial Hemorrhage Study was a clinical trial supported by the National Institute of Neurological and Communicative Disorders and Stroke (NINCDS), and enrolled 280 infants at three Harvard Neonatal Intensive Care Units between June 1981 and April 1984. Babies were recruited for the study if their birth weights were 1,750 grams or less, they had no demonstrable intraventricular hemorrhage by cranial ultrasound and they required intubation within the first twelve hours of life. Data collected included maternal history, infant health status, and events of hospitalization.
The Antenatal Risk Factors for Intraventricular Hemorrhage Study, also funded by NINCDS, was composed of 520 infants, at or less than 1,500 grams birth weight who were born at two Harvard teaching hospitals between July 1984 and September 1986. Babies were enrolled if they were alive when their mothers were interviewed, usually 24-48 hours after delivery. Procedures in the delivery room and findings on early examinations were recorded. Information about the first five days of life was collected daily.
Bronchopulmonary dysplasia/chronic pulmonary disease of prematurity is a substantial long-term problem in survivors of neonatal intensive care. This disorder is seen in 15 to 35 percent of surviving infants whose birth weight was less than 1,500 grams. It is estimated that 5 percent of all neonatal intensive care unit admissions develop the affliction. Affected infants require prolonged neonatal intensive care unit (NICU) hospitalizations.
When the study was begun in 1988, infants with BPD who survived to NICU discharge required home oxygen therapy for months to years. In addition, they had a 50-69 percent chance of re-hospitalization and an 11-36 percent probability of death in the first year of life. Although improvement with age was often seen, pulmonary function abnormalities persisted into late childhood or beyond in at least 75 percent. Among other associated morbid sequelae were myocardial and pulmonary vascular dysfunction, cor pulmonale, systemic hypertension, growth failure, and neurodevelopmental abnormalities. Pathologic studies showed structural pulmonary and myocardial abnormalities in the most severely affected infants.
Of advances in the field of neonatology, one of the most exciting was the experimental use of exogenous surfactant. Neonatal clinicians and researchers looked to these preparations for specific therapy for hyaline membrane disease and indirect reduction of neonatal mortality and chronic pulmonary disease of prematurity. Published clinical studies of exogenous surfactant were supportive of the anticipated trends in neonatal mortality and morbidity. Up to 1988, however, surfactant therapy was shown to have a more appreciable impact on acute respiratory disease and neonatal mortality than on the rate of bronchopulmonary dysplasia. Unfortunately, published trials reported that even surfactant-treated premature infants developed fatal bronchopulmonary dysplasia.
DESIGN NARRATIVE:
The design was that of a retrospective, case-control study. The populations of babies studied in the Phenobarbital Study and the Antenatal Risk Factor Study were not identical and therefore, were not combined for analysis but allowed hypotheses generated in one sample to be tested in the other. In a review of medical records, cases were chosen based on the clinical criterion of a requirement for supplemental oxygen for 28 days or more. An additional requirement for case status was the presence of classical stages II, III, or IV radiographic findings of bronchopulmonary dysplasia/chronic pulmonary disease of prematurity. Positive readings by two independent pediatric radiologists were required for case assignment. Control infants were those who failed to meet case criteria. Hypothesis testing proceeded from univariate to stratified analyses and, finally, to multivariate modeling. Candidates for multivariate analysis included: antenatal factors such as maternal age, race, marital status, obstetric history and pregnancy history; perinatal factors such as birth weight, gestational age, degree of illness; neonatal factors such as respiratory condition, body fluids, and miscellaneous laboratory data.
The study completion date listed in this record was obtained from the "End Date" entered in the Protocol Registration and Results System (PRS) record.
- Conditions
- Lung Diseases, Bronchopulmonary Dysplasia
- Medical subject headings
- Lung Diseases, Bronchopulmonary Dysplasia
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted26 May 2000 (estimated)
- Study startDec 1988
- Study completionNov 1990
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Publications (3)Papers the sponsor has linked to this study.
- Other trials for Lung DiseasesStudies of the same condition, open and under way.
- More trials run by National Heart, Lung, and Blood Institute (NHLBI)The sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Observational
Sponsor and investigators
- Sponsor type
- US National Institutes of Health
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT00005293
- Sponsor's protocol ID
- 2015
- Other IDs
- R01HL040454
- Status last verified
- Apr 2000
- First submitted
- 25 May 2000
- Last updated
- 16 Mar 2016
- Results posted
- No
Publications
Van Marter LJ, Leviton A, Kuban KC, Pagano M, Allred EN. Maternal glucocorticoid therapy and reduced risk of bronchopulmonary dysplasia. Pediatrics. 1990 Sep;86(3):331-6.
PubMed 2201940Van Marter LJ, Leviton A, Allred EN, Pagano M, Kuban KC. Hydration during the first days of life and the risk of bronchopulmonary dysplasia in low birth weight infants. J Pediatr. 1990 Jun;116(6):942-9. doi: 10.1016/s0022-3476(05)80658-4.
PubMed 2189976Van Marter LJ, Pagano M, Allred EN, Leviton A, Kuban KC. Rate of bronchopulmonary dysplasia as a function of neonatal intensive care practices. J Pediatr. 1992 Jun;120(6):938-46. doi: 10.1016/s0022-3476(05)81968-7.
PubMed 1593356
Study at a glance
From the registry record, last updated by the sponsor on 16 Mar 2016. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- Antecedents of Bronchopulmonary Dysplasia
- ClinicalTrials.gov ID
- NCT00005293
- Acronym / sponsor ID
- 2015
- Conditions
- Lung Diseases, Bronchopulmonary Dysplasia
- Study type
- Observational
- Recruitment status
- Completed
- Lead sponsor
- National Heart, Lung, and Blood Institute (NHLBI)US National Institutes of Health
- Study start
- Dec 1988
- Study completion
- Nov 1990 (actual)
- First posted
- 26 May 2000 (estimated)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
To identify risk factors for bronchopulmonary dysplasia/chronic pulmonary disease of prematurity and to estimate proportions of this group of disorders attributable to antenatal risk factors, perinatal events, and neonatal care procedures.
Detailed description
BACKGROUND:
The Phenobarbital Prophylaxis for Neonatal Intracranial Hemorrhage Study was a clinical trial supported by the National Institute of Neurological and Communicative Disorders and Stroke (NINCDS), and enrolled 280 infants at three Harvard Neonatal Intensive Care Units between June 1981 and April 1984. Babies were recruited for the study if their birth weights were 1,750 grams or less, they had no demonstrable intraventricular hemorrhage by cranial ultrasound and they required intubation within the first twelve hours of life. Data collected included maternal history, infant health status, and events of hospitalization.
The Antenatal Risk Factors for Intraventricular Hemorrhage Study, also funded by NINCDS, was composed of 520 infants, at or less than 1,500 grams birth weight who were born at two Harvard teaching hospitals between July 1984 and September 1986. Babies were enrolled if they were alive when their mothers were interviewed, usually 24-48 hours after delivery. Procedures in the delivery room and findings on early examinations were recorded. Information about the first five days of life was collected daily.
Bronchopulmonary dysplasia/chronic pulmonary disease of prematurity is a substantial long-term problem in survivors of neonatal intensive care. This disorder is seen in 15 to 35 percent of surviving infants whose birth weight was less than 1,500 grams. It is estimated that 5 percent of all neonatal intensive care unit admissions develop the affliction. Affected infants require prolonged neonatal intensive care unit (NICU) hospitalizations.
When the study was begun in 1988, infants with BPD who survived to NICU discharge required home oxygen therapy for months to years. In addition, they had a 50-69 percent chance of re-hospitalization and an 11-36 percent probability of death in the first year of life. Although improvement with age was often seen, pulmonary function abnormalities persisted into late childhood or beyond in at least 75 percent. Among other associated morbid sequelae were myocardial and pulmonary vascular dysfunction, cor pulmonale, systemic hypertension, growth failure, and neurodevelopmental abnormalities. Pathologic studies showed structural pulmonary and myocardial abnormalities in the most severely affected infants.
Of advances in the field of neonatology, one of the most exciting was the experimental use of exogenous surfactant. Neonatal clinicians and researchers looked to these preparations for specific therapy for hyaline membrane disease and indirect reduction of neonatal mortality and chronic pulmonary disease of prematurity. Published clinical studies of exogenous surfactant were supportive of the anticipated trends in neonatal mortality and morbidity. Up to 1988, however, surfactant therapy was shown to have a more appreciable impact on acute respiratory disease and neonatal mortality than on the rate of bronchopulmonary dysplasia. Unfortunately, published trials reported that even surfactant-treated premature infants developed fatal bronchopulmonary dysplasia.
DESIGN NARRATIVE:
The design was that of a retrospective, case-control study. The populations of babies studied in the Phenobarbital Study and the Antenatal Risk Factor Study were not identical and therefore, were not combined for analysis but allowed hypotheses generated in one sample to be tested in the other. In a review of medical records, cases were chosen based on the clinical criterion of a requirement for supplemental oxygen for 28 days or more. An additional requirement for case status was the presence of classical stages II, III, or IV radiographic findings of bronchopulmonary dysplasia/chronic pulmonary disease of prematurity. Positive readings by two independent pediatric radiologists were required for case assignment. Control infants were those who failed to meet case criteria. Hypothesis testing proceeded from univariate to stratified analyses and, finally, to multivariate modeling. Candidates for multivariate analysis included: antenatal factors such as maternal age, race, marital status, obstetric history and pregnancy history; perinatal factors such as birth weight, gestational age, degree of illness; neonatal factors such as respiratory condition, body fluids, and miscellaneous laboratory data.
The study completion date listed in this record was obtained from the "End Date" entered in the Protocol Registration and Results System (PRS) record.
Study design
Who may qualify
- Ages
- Up to 100 years
- Sex
- Male only
- Healthy volunteers
- Not accepted
- Age groups
- Child, Adult, Older adult
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Primary outcome
Not reported in the source record.
Results and safety
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 16 Mar 2016.
- Background: PubMed 2201940Van Marter LJ, Leviton A, Kuban KC, Pagano M, Allred EN. Maternal glucocorticoid therapy and reduced risk of bronchopulmonary dysplasia. Pediatrics. 1990 Sep;86(3):331-6.
- Background: PubMed 2189976Van Marter LJ, Leviton A, Allred EN, Pagano M, Kuban KC. Hydration during the first days of life and the risk of bronchopulmonary dysplasia in low birth weight infants. J Pediatr. 1990 Jun;116(6):942-9. doi: 10.1016/s0022-3476(05)80658-4.
- Background: PubMed 1593356Van Marter LJ, Pagano M, Allred EN, Leviton A, Kuban KC. Rate of bronchopulmonary dysplasia as a function of neonatal intensive care practices. J Pediatr. 1992 Jun;120(6):938-46. doi: 10.1016/s0022-3476(05)81968-7.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part. This study is not recruiting at the moment.
The record lists no contact. Use the official record to reach the sponsor.
Questions about this trial
What is this clinical trial studying?
An observational study of Lung Diseases and Bronchopulmonary Dysplasia, run by National Heart, Lung, and Blood Institute (NHLBI).
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: finished, as of the sponsor's last update on 16 Mar 2016. Status can change between updates, so confirm with the study contact before making plans.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
Are results available for this study?
The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.
How can a doctor refer a patient or contact the research team?
The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.
Where can I read the original study information?
On the ClinicalTrials.gov record for NCT00005293, which also lists 3 linked publications.
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 16 Mar 2016.