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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
National Heart, Lung, and Blood Institute (NHLBI)
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional prevention trial for Lung Diseases

Eligibility Criteria

undefined - 1 Year (Child)All SexesDoes not accept healthy volunteers

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

    First Posted
    October 27, 1999
    Last Updated
    April 26, 2012
    Sponsor
    National Heart, Lung, and Blood Institute (NHLBI)
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    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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