Clinical trial

fFN & E3 in the Prediction of PTB in Women With Twin Pregnancies Receiving 17OHP…

NCT00156000 · Obstetrix Medical Group, Industry · Withdrawn

Key facts

NCT number NCT00156000
Title fFN & E3 in the Prediction of PTB in Women With Twin Pregnancies Receiving 17OHP or Placebo
Official title Fetal Fibronectin (fFN) and Salivary Estriol (E3) in the Prediction of Preterm Birth in Women With Twin Pregnancies Receiving 17-Alpha-Hydroxyprogesterone Caproate or Placebo
Lead sponsor Obstetrix Medical Group, Industry
Collaborators Adeza Biomedical Industry
Status Withdrawn
Study type Observational
Conditions Preterm Delivery, Preterm Birth
Intervention type Device
Interventions Fetal Fibronectin, Salivary Estriol
Enrollment 0
Start date Aug 1, 2005
Primary completion Feb 1, 2006
Completion Feb 1, 2006
First posted Sep 12, 2005
Last update posted Dec 19, 2014
Countries United States

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

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

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

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