Clinical trial

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

NCT00163020 · Obstetrix Medical Group, Industry · Completed

Key facts

NCT number NCT00163020
Title 17OHP for Reduction of Neonatal Morbidity Due to Preterm Birth (PTB) in Twin and Triplet Pregnancies
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
Acronym 170HP
Lead sponsor Obstetrix Medical Group, Industry
Status Completed
Phase Phase 2/Phase 3
Study type Interventional
Conditions Preterm Birth
Intervention type Drug
Interventions 17-alpha-hydroxyprogesterone caproate injectable, Placebo
Enrollment 321
Start date Nov 1, 2004
Primary completion Aug 1, 2009
Completion Aug 1, 2009
First posted Sep 13, 2005
Last update posted Apr 11, 2016
Countries United States

At a glance

  • 10–99 Study sites
  • Yes Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About ClinicalTrials.gov studies

ClinicalTrials.gov is the U.S. National Library of Medicine's registry of clinical studies conducted around the world. Contact and investigator details are not shown here.

Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

Browse all ClinicalTrials.gov studies