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A Multicenter Assessment of a Spontaneous Preterm Birth Risk Predictor — TREETOP  

Preterm Birth Clinical Trial

Official title:
A Multicenter Assessment of a Spontaneous Preterm Birth Risk Predictor

Clinical Trial Summary

Prospective multicenter observational study to further develop and validate a preterm birth risk predictor, using a preterm cutoff at 37 0/7 weeks gestation and at 35 0/7 weeks gestation. A single maternal peripheral blood sample will be collected for analysis. Data related to potential risk factors for preterm birth will be obtained through maternal interview and review of medical records. Subjects will be followed through the delivery process to assess the course of pregnancy, labor, and to document any related maternal complications. Neonatal outcomes will be gathered from the medical record for up to 28 days of life or discharge, whichever occurs first.

Clinical Trial Description

n/a

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02787213
Study type Observational
Source Sera Prognostics, Inc.
Contact
Status Completed
Phase
Start date August 2016
Completion date June 2019
View Details
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