Non Invasive Biomarkers to Identify Subjects at Risk for Preterm Delivery

Stopped early

Conditions studied: Preterm Birth

In brief

The goal of this study is to identify a non-invasive predictor or predictors that will increase the clinician's ability to identify patients with preterm labor (PTL) at risk for preterm delivery (PTD). Through these studies we also hope to reveal potential therapeutic targets in the prevention of prevention of preterm births. The study hypothesis is that we can identify non-invasive predictors of PTL at risk for PTD.

Key facts

Study ID

NCT00919412

Run by

NYU Langone Health

People needed

32

Starts

2007-06-01

Expected to finish

2010-09-01

Last updated by the study team

2020-05-13

Who can join

Age: 18 and older, up to 45. Sex: female. Healthy volunteers: not accepted.

You may qualify if…

• Women with a diagnosis of preterm labor.

You may not qualify if…

• Multiple pregnancy, fetal anomalies, abruptio placenta, preeclampsia, cervical dilation greater than 4 cm, clinical signs of infection and vaginal bleeding

Where it is running

• Winthrop-University Hospital — Mineola, New York, United States

Full record on ClinicalTrials.gov

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