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Completed Phase 2Phase 3 Interventional Results available

17OHP for Reduction of Neonatal Morbidity Due to Preterm Birth (PTB) in Twin and Triplet Pregnancies

ClinicalTrials.gov ID: NCT00163020

Public ClinicalTrials.gov record NCT00163020. 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 Jul 21, 2026, 11:23 AM EDT

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

Official title

17-Alpha-Hydroxyprogesterone Caproate for Reduction of Neonatal Morbidity Due to Preterm Birth in Twin and Triplet Pregnancies - A Concurrent Randomized Double-blinded Clinical Trial

Study identification

NCT ID
NCT00163020
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2, Phase 3
Lead sponsor
Obstetrix Medical Group
Industry
Enrollment
321 participants

Conditions and interventions

Conditions

Interventions

  • 17-alpha-hydroxyprogesterone caproate injectable Drug
  • Placebo Drug

Drug

Eligibility (public fields only)

Age range
18 Years to 65 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, 2004
Primary completion
Jul 31, 2009
Completion
Jul 31, 2009
Last update posted
Apr 10, 2016

2004 – 2009

United States locations

U.S. sites
18
U.S. states
8
U.S. cities
16
Facility City State ZIP Site status
Banner Good Samaritan 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 Southern 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
Saint Luke's Hospital, Kansas City Kansas City Missouri 64111
Erlanger Medical Center Chattanooga Tennessee 37403
Baylor University Medical Center Dallas Texas 75246
Harris Methodist Fort Worth Hospital Fort Worth Texas 76104
Evergreen Hospital Kirkland Washington 98034
Swedish Medical Center Seattle Washington 98122-4307
Tacoma General Hospital Tacoma Washington 98405

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 NCT00163020, 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 Apr 10, 2016 · Synced Jul 21, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT00163020 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →