Prevention of Neonatal Respiratory Distress Syndrome With Antenatal Steroid Administration
Primary Purpose
Lung Diseases, Respiratory Distress Syndrome
Status
Completed
Phase
Phase 3
Locations
Study Type
Interventional
Intervention
dexamethasone
Sponsored by
About this trial
This is an interventional prevention trial for Lung Diseases
Eligibility Criteria
Male and female fetuses and infants; pregnant women with anticipated premature delivery and gestational age between 26 and 37 weeks.
Sites / Locations
Outcomes
Primary Outcome Measures
Secondary Outcome Measures
Full Information
NCT ID
NCT00000563
First Posted
October 27, 1999
Last Updated
April 26, 2012
Sponsor
National Heart, Lung, and Blood Institute (NHLBI)
1. Study Identification
Unique Protocol Identification Number
NCT00000563
Brief Title
Prevention of Neonatal Respiratory Distress Syndrome With Antenatal Steroid Administration
Study Type
Interventional
2. Study Status
Record Verification Date
April 2012
Overall Recruitment Status
Completed
Study Start Date
June 1976 (undefined)
Primary Completion Date
undefined (undefined)
Study Completion Date
August 1983 (Actual)
3. Sponsor/Collaborators
Name of the Sponsor
National Heart, Lung, and Blood Institute (NHLBI)
4. Oversight
5. Study Description
Brief Summary
To determine the effect of corticosteroids, administered 24 to 48 hours before parturition, on the incidence of neonatal respiratory distress syndrome (RDS) and to determine whether the therapy has any adverse short- or long-term (up to 36 months) effects on the infant. Secondarily, to determine whether the therapy has any adverse short-term effects on the mother and to determine whether morbidity rates for neonatal respiratory distress syndrome as well as total and cause-specific infant mortality rates differ between mothers who received antenatal steroids and those who received conventional medical care.
Detailed Description
BACKGROUND:
Neonatal respiratory distress syndrome is one of the leading causes of disability and death in the newborn. In the United States, approximately 10 percent of all infants are premature, and each year about 50,000 cases of neonatal respiratory distress syndrome occur.
Extensive studies in animal models on respiratory distress syndrome have demonstrated that antenatal administration of synthetic (dexamethasone) and natural (cortisol) corticosteroids accelerates lung maturation and significantly diminishes the occurrence of RDS. Although a variety of conditions in newborn infants have been treated with steroids over the past 20 years without adverse effects, investigations have been needed on the short-term effects of corticosteroids administered antenatally on neonate and mother and on the long-term effects on the infant.
The Planning Phase of this trial was completed in March 1977, with formulation of a common protocol and manual of operations. Patient screening and enrollment began in August 1977 and ended on March 1, 1980. Follow-up ended in August 1983 and data analysis was completed October 31, 1983.
DESIGN NARRATIVE:
Randomized, double-blind, fixed sample. Six hundred and ninety-six pregnant women were randomized to four doses of dexamethasone every 12 hours or to placebo. Endpoints were the incidence of respiratory distress syndrome and abnormality of motor-neuro-intellectual development in their infants.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Lung Diseases, Respiratory Distress Syndrome
7. Study Design
Primary Purpose
Prevention
Study Phase
Phase 3
Masking
Double
Allocation
Randomized
8. Arms, Groups, and Interventions
Intervention Type
Drug
Intervention Name(s)
dexamethasone
10. Eligibility
Sex
All
Maximum Age & Unit of Time
1 Year
Accepts Healthy Volunteers
No
Eligibility Criteria
Male and female fetuses and infants; pregnant women with anticipated premature delivery and gestational age between 26 and 37 weeks.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Charles Bauer
Organizational Affiliation
University of Miami
First Name & Middle Initial & Last Name & Degree
Richard Depp
Organizational Affiliation
Northwestern University
First Name & Middle Initial & Last Name & Degree
Sheldon Korones
Organizational Affiliation
University of Tennessee
First Name & Middle Initial & Last Name & Degree
Henrique Rigatto
Organizational Affiliation
University of Manitoba
First Name & Middle Initial & Last Name & Degree
Richard Zachman
Organizational Affiliation
University of Wisconsin, Madison
12. IPD Sharing Statement
Citations:
PubMed Identifier
7025638
Citation
Effect of antenatal dexamethasone administration on the prevention of respiratory distress syndrome. Am J Obstet Gynecol. 1981 Oct 1;141(3):276-87.
Results Reference
background
PubMed Identifier
6363659
Citation
Effects of antenatal dexamethasone administration in the infant: long-term follow-up. J Pediatr. 1984 Feb;104(2):259-67. doi: 10.1016/s0022-3476(84)81009-4.
Results Reference
background
Citation
Collaborative Group on Antenatal Steroid Therapy: Prevention of Respiratory Distress Syndrome: Effect of Antenatal Dexamethasone Administration. Hospital and Follow-up Studies. NIH Publication No. 85-2695, 1985.
Results Reference
background
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Prevention of Neonatal Respiratory Distress Syndrome With Antenatal Steroid Administration
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