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Terminated Phase 3 Interventional Accepts healthy volunteers

Repeat Antenatal Steroids Trial

ClinicalTrials.gov ID: NCT00015002

Public ClinicalTrials.gov record NCT00015002. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 28, 2026, 3:30 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomized Placebo-Controlled Trial of Antenatal Corticosteroid Regimens

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A course of steroids given to a mother who is in labor with a premature fetus will reduce the risk of the premature infant dying or having serious complications. This trial will test whether more than one course of antenatal steroids is more beneficial or risky to the infant than a single course.

Study identification

NCT ID
NCT00015002
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Enrollment
486 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
Not listed
Sex
Female
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 2000 (Type not available)
Primary completion
May 2006 (Actual)
Completion
Mar 2007 (Actual)
Last update posted
Mar 31, 2022

2000 – 2007

United States locations

U.S. sites
19
U.S. states
12
U.S. cities
18
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35294 —
University of Miami Miami Florida 33136 —
Northwestern University-Prentice Hospital Chicago Illinois 60611 —
University of Chicago Chicago Illinois 60637 —
Dept of OB/GYN, Hutzel Hospital Detroit Michigan 48201 —
Columbia University New York New York 10032 —
University of North Carolina Chapel Hill North Carolina 27599 —
Forsyth Memorial Hospital, Wake Forest University School of Medicine Winston-Salem North Carolina 27103 —
University of Cincinnati Cincinnati Ohio 45267 —
Case Western Reserve-Metrohealth Cleveland Ohio 44109 —
Dept of OB/GYN, Ohio State University Columbus Ohio 43210 —
MCP Hahnamann Philadelphia Pennsylvania 19102 —
Dept of OB/GYN, Magee-Womens Hospital Pittsburgh Pennsylvania 15213 —
Brown University -Women and Infants Hospital Providence Rhode Island 02095 —
University of Tennessee Memphis Tennessee 38103 —
Dept of OB/GYN, Southwestern Medical Center, University of Texas Dallas Texas 75235-9032 —
University of Texas-Houston Houston Texas 77030 —
University of Texas - San Antonio San Antonio Texas 78284 —
University of Utah Medical Center Salt Lake City Utah 84132 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00015002, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 31, 2022 · Synced Oct 28, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00015002 live on ClinicalTrials.gov.

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