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UnknownNCT01955148

fFN Clinical Evaluation in Asymptomatic Women at High Risk for Preterm Birth

Prospective Phase III Evaluation Of Fetal Fibronectin In A High Risk Asymptomatic Population For The Prediction Of Spontaneous Preterm Birth

Status
Unknown
Phase
Study type
Observational
Enrollment
1,210 (estimated)
Sponsor
Hologic, Inc. · Industry
Sex
Female
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

This study is designed to determine if quantitative analysis of fetal Fibronectin (fFN) can be used to advance prediction of spontaneous preterm birth (sPTB). This will be a prospective observational multi-center study with approximately 15 to 20 US sites, and approximately 1210 subjects evaluating the clinical utility of the Rapid fFN 10Q system for preterm birth risk assessment. A single fFN specimen will be collected from each subject between 16 weeks, 0 days and 21 weeks, 6 days. The primary and secondary maternal outcome measures will be determined based on the date of delivery and the estimated date of confinement (EDC), which will be evaluated in a standardized manner.

Detailed description

Hologic has developed a quantitative test to assess the amount of fetal fibronectin (fFN) present in cervicovaginal secretions, and evaluate the clinical utility of the test in assessing spontaneous Pre-Term Bith risk in a high risk population. Identifying women at high risk of giving birth prematurely can be challenging. It is believed that higher levels of fFn measured in vaginal fluid suggest a woman is at a greater risk for delivering early. fFN testing is already approved for use in women from weeks 22 to 35 of pregnancy. The goal of this study is to evaluate the benefits of collecting fFN measurements from a vaginal fluid specimen taken during early pregnancy (from 16 weeks to 22 weeks) to assess the risk of pre-term birth.

Conditions

Timeline

Start date
2013-10-01
Primary completion
2016-07-01
Completion
2016-09-01
First posted
2013-10-07
Last updated
2015-08-26

Locations

16 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01955148. Inclusion in this directory is not an endorsement.