Randomized Trial of Hydrocortisone in Very Preterm High-Risk Infants
Information source: The University of Texas Health Science Center, Houston
Information obtained from ClinicalTrials.gov on February 12, 2009 Link to the current ClinicalTrials.gov record.
Condition(s) targeted: Bronchopulmonary Dysplasia; Encephalomalacia; Premature Birth
Intervention: Hydrocortisone (Drug); Placebo (Drug)
Phase: Phase 2
Status: Recruiting
Sponsored by: The University of Texas Health Science Center, Houston Official(s) and/or principal investigator(s): Nehal A. Parikh, D.O., Principal Investigator, Affiliation: University of Texas Health Science Center Medical School at Houston
Overall contact: Georgia E. McDavid, RN, Phone: 713-500-5734, Email: Georgia.E.Mcdavid@uth.tmc.edu
Summary
The purpose of this study is to determine whether treatment of very preterm infants at
high-risk for lung and brain injury with low dose hydrocortisone results in improved
pulmonary and neurologic outcomes.
Clinical Details
Official title: A Randomized Trial of Hydrocortisone in Very Preterm Infants at High Risk for Neurologic and Pulmonary Impairments
Study design: Prevention, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Parallel Assignment, Safety/Efficacy Study
Primary outcome: Total cerebral volume as measured by volumetric brain MRI
Secondary outcome: Regional brain volumesDuration of mechanical ventilation Duration of oxygen requirement Diagnosis of BPD
Detailed description:
Hypothesis: Among extremely low birth weight infants (ELBW; BW ≤ 1000 g) at high risk for
bronchopulmonary dysplasia (BPD) and neurologic impairments, those infants randomized to
seven days of hydrocortisone will demonstrate increased total cerebral tissue volumes as
compared to infants randomized to placebo.
Specific Aims: 1) To perform a pilot blinded randomized controlled trial of a 7-day regimen
of low dose hydrocortisone in ELBW infants at high risk for BPD and neurosensory impairments
and assess its effect on cerebral tissue volumes. 2) Evaluate and report 2 year
neurodevelopmental outcomes.
Background and Significance: Bronchopulmonary dysplasia is a disease of arrested lung
development and lung inflammation. It is primarily seen in ELBW infants. Neurological
delay, including cerebral palsy and mental retardation, affect up to 40%-50% of surviving
ELBW infants. BPD is an important risk factor for such neurological delay. Postnatal
administration of corticosteroids to ventilated preterm neonates results in a reduced risk of
developing BPD. Postnatal corticosteroids however have shown harmful effects on the brain
and can lead to increased rates of cerebral palsy and learning problems. This effect has
primarily been seen with dexamethasone when high doses were given in the first week of life.
Beyond the first week of life, there is insufficient information on the effects of steroids
on the brain. Steroids other than dexamethasone, in much lower doses have been shown to
improve short term lung function with minimal short-term side effects. A review study of all
steroid trials for BPD shows that when given to a high risk group of infants (> 50% risk of
BPD) steroids protect the brain and reduce rates of cerebral palsy. The American and
Canadian Pediatric societies and respected researchers have commented on the urgent need for
more trials of other corticosteroids at lower doses started after the first week of life to
evaluate their short and long-term pulmonary and neurological benefits and risks.
Research Design and Methods:
1. Inclusion & Exclusion Criteria: See below.
2. Procedures: Consented eligible patients will be randomly assigned to receive
hydrocortisone in a tapering schedule over 7 days or placebo (comparison group). Study
drug will be given every 12 hours IV with only study pharmacist aware of assignment.
The patient's anatomic brain MRI (routinely done on all ELBW infants at 38 weeks
post-menstrual age) will be further processed by the masked study investigators to
derive total and regional brain volumes. Administration of indomethacin or
dexamethasone to enrolled infants will be closely monitored and regulated throughout the
trial period. Indomethacin use during study period is contraindicated. Dexamethasone
(or other steroid) use will be restricted to ELBW infants on high ventilator settings
(RIS > 10) after 28 days of life. All other procedures will be per routine care.
Blinded developmental follow-up at two years, already currently performed for all ELBW
infants at MHCH, will be analyzed and reported for all study infants.
Eligibility
Minimum age: N/A.
Maximum age: 3 Weeks.
Gender(s): Both.
Criteria:
Inclusion Criteria:
- Patient in the Memorial Hermann Children's Hospital (MHCH) NICU with a birth weight â¤
1000 grams.
- Ventilator-dependent between 10 and 21 days of age.
- Respiratory index score (RIS: mean airway pressure x fraction of inspired oxygen) of â¥
2. 0 that is increasing or stable for the previous 24 hours or a RIS ⥠3. 0 if
improvement noted in the past 24 hours.
Exclusion Criteria:
- Prior postnatal steroid treatment.
- Evidence of sepsis or necrotizing enterocolitis.
- Known major congenital anomalies of the cardiopulmonary or central nervous system.
- Infants being treated with indomethacin or those likely to require treatment in the
next 7 days as judged by the treating physician.
- Inability or unwillingness of parent or legal guardian/representative to give written
informed consent.
- Gestational age < 23 weeks.
Locations and Contacts
Georgia E. McDavid, RN, Phone: 713-500-5734, Email: Georgia.E.Mcdavid@uth.tmc.edu
Memorial Hermann Children's Hospital, Houston, Texas 77030, United States; Recruiting Marianna Riggs, Phone: 713-704-4256, Email: Marianna_Riggs@mhhs.org Joy Lilljedahl, MBA, Phone: 713-704-4269, Email: Joy.C.Lilljedahl@uth.tmc.edu Jon E Tyson, MD, MPH, Sub-Investigator Kathleen A. Kennedy, MD, MPH, Sub-Investigator Nehal A. Parikh, D.O., Principal Investigator
Additional Information
Patient information page - Bronchopulmonary Dysplasia
Related publications: Parikh NA, Lasky RE, Kennedy KA, Moya FR, Hochhauser L, Romo S, Tyson JE. Postnatal dexamethasone therapy and cerebral tissue volumes in extremely low birth weight infants. Pediatrics. 2007 Feb;119(2):265-72.
Starting date: November 2005
Ending date: May 2010
Last updated: October 22, 2008
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