Proteomic Assessment of Preterm Birth

NCT01371019 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 5500

Last updated 2015-06-11

No results posted yet for this study

Summary

The purpose of this study is to to collect and store blood samples that will be utilized to develop a multimarker test to predict preterm delivery.

Conditions

Sponsors & Collaborators

  • Sera Prognostics, Inc.

    lead INDUSTRY

Principal Investigators

  • Durlin E Hickok, MD, MPH · Sera Prognostics, Inc.

Eligibility

Min Age
18 Years
Max Age
60 Years
Sex
FEMALE
Healthy Volunteers
No

Timeline & Regulatory

Start
2011-04-30
Primary Completion
2014-12-31
Completion
2015-04-30

Countries

  • United States

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT01371019 on ClinicalTrials.gov