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Prospective Evaluation of Pathways for Preterm Birth

NCT05246579 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 240

Last updated 2025-07-02

No results posted yet for this study

Summary

This is a single center, prospective cohort study of pregnant patients at high risk for spontaneous preterm birth: patient's with history of spontaneous preterm birth, patient's with a short cervix and patient's symptomatic for preterm birth will be included. A control cohort of nulliparous patients without a short cervix will be recruited to provide baseline data. Plan to enroll 240 patients identified through our ultrasound unit with goal of 60 patients in each group.

Conditions

Sponsors & Collaborators

  • John O'Brien, MD

    lead OTHER

Principal Investigators

  • John O'Brien, MD · University of Kentucky

Eligibility

Min Age
18 Years
Max Age
45 Years
Sex
FEMALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2022-02-04
Primary Completion
2026-06-01
Completion
2026-06-01

Countries

  • United States

Study Locations

More Related Trials

Entities

Diseases

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 NCT05246579 on ClinicalTrials.gov