Status:
TERMINATED
Non Invasive Biomarkers to Identify Subjects at Risk for Preterm Delivery
Lead Sponsor:
NYU Langone Health
Conditions:
Preterm Birth
Eligibility:
FEMALE
18-45 years
Brief Summary
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)...
Detailed Description
STUDY DESIGN This is a prospective study involving a cohort of pregnant subjects with pre-term labor. Maternal blood and cervical/vaginal fluid will be collected from consenting subjects with preterm ...
Eligibility Criteria
Inclusion
- Women with a diagnosis of preterm labor.
Exclusion
- Multiple pregnancy, fetal anomalies, abruptio placenta, preeclampsia, cervical dilation greater than 4 cm, clinical signs of infection and vaginal bleeding
Key Trial Info
Start Date :
June 1 2007
Trial Type :
OBSERVATIONAL
Allocation :
ACTUAL
End Date :
September 1 2010
Estimated Enrollment :
32 Patients enrolled
Trial Details
Trial ID
NCT00919412
Start Date
June 1 2007
End Date
September 1 2010
Last Update
May 13 2020
Active Locations (1)
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1
Winthrop-University Hospital
Mineola, New York, United States, 11501