ClinicalTrials.gov record
Completed Phase 4 Interventional Results available

A Randomized Trial Comparing the Impact of One Versus Two Courses of Antenatal Steroids (ACS) on Neonatal Outcome

ClinicalTrials.gov ID: NCT00201643

Public ClinicalTrials.gov record NCT00201643. 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 May 6, 2026, 6:30 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 Double-Blinded Study Comparing the Impact of One Versus Two Courses of Antenatal Steroids on Neonatal Outcome

Study identification

NCT ID
NCT00201643
Recruitment status
Completed
Study type
Interventional
Phase
Phase 4
Lead sponsor
Obstetrix Medical Group
Industry
Enrollment
437 participants

Conditions and interventions

Interventions

  • Betamethasone or Dexamethasone (2nd course of ACS) Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 60 Years
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

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

Study timeline

Start date
Oct 31, 2003
Primary completion
Jan 31, 2008
Completion
Jan 31, 2008
Last update posted
Jan 6, 2015

2003 – 2008

United States locations

U.S. sites
22
U.S. states
10
U.S. cities
19
Facility City State ZIP Site status
Desert Good Samaritan Hospital Mesa Arizona 85202
Banner Good Sammaritan Hospital Phoenix Arizona 85006
Tucson Medical Center Tucson Arizona 85712
Saddleback Memorial Medical Center Laguna Hills California 92653
Long Beach Memorial Medical Center Long Beach California 90801-1428
University of Sourthern California-Irvine Medical Center Orange California 92868
Good Samaritan Hospital San Jose California 95124
Swedish Medical Center Denver Colorado 80110
Presbyterian/St Luke's Hospital Denver Colorado 80218
Rose Medical Center Denver Colorado 80220
Skyridge Medical Center Lonetree Colorado 80124
Mercy Medical Center Des Moines Iowa 50314
Tufts-New England Medical Center Boston Massachusetts 02111
Saint Luke's Hospital, Kansas City Kansas City Missouri 64111
Saint John's Regional Health Center Springfield Missouri 65804
University Med. Ctr. of Southern Nevada Las Vegas Nevada 89102
Sunrise Medical Center Las Vegas Nevada 89109
Erlanger Medical Center Chattanooga Tennessee 37403
University of Tennessee Medical Center Knoxville Tennessee 37920
University of Utah Health Sciences Center Salt Lake City Utah 84132
Evergreen Hospital Kirkland Washington 98034
Swedish Medical Center Seattle Washington 98122-4307

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 NCT00201643, 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 Jan 6, 2015 · Synced May 6, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00201643 live on ClinicalTrials.gov.

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