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Clinical trialNCT02518594CompletedPhase 3Interventional

A Trial of Pessary and Progesterone for Preterm Prevention in Twin Gestation With a Short Cervix

SponsorThe George Washington University Biostatistics CenterEnrollment1,311Short Cervical Length
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

This protocol outlines a randomized trial of 630 women evaluating the use of micronized vaginal progesterone or pessary versus control (placebo) to prevent early preterm birth in women carrying twins and with a cervical length of less than 30 millimeters.

Investigators

The overall officials registered on this study. Names that resolve to a findmyKOL profile link to it; the rest are shown as registered.

  • Joseph Biggio, MD

    Maternal Fetal Medicine Units (MFMU) Network

    Study Chair
  • Monica Longo, MD

    Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)

    Study Director

A profile link is shown only when the registered name resolves to a person record with a confident, namesake-checked match; ambiguous names stay unlinked.

Sites

16 registered facilities, with the per-site recruitment status where the registry publishes one. ClinicalTrials.gov does not publish per-site enrollment counts.

United States
  • University of Alabama - Birmingham

    Birmingham, Alabama, United States

  • the Regents of the University of California, San Francisco

    San Francisco, California, United States

  • University of Colorado

    Denver, Colorado, United States

  • Northwestern University-Prentice Hospital

    Chicago, Illinois, United States

  • Columbia University

    New York, New York, United States

  • University of North Carolina - Chapel Hill

    Chapel Hill, North Carolina, United States

  • Duke University

    Durham, North Carolina, United States

  • Case Western Reserve University

    Cleveland, Ohio, United States

  • Ohio State University

    Columbus, Ohio, United States

  • Hospital of the University of Pennsylvania

    Philadelphia, Pennsylvania, United States

  • Magee Women'S Hospital

    Pittsburgh, Pennsylvania, United States

  • Brown University

    Providence, Rhode Island, United States

  • University of Texas - Galveston

    Galveston, Texas, United States

  • Baylor College of Medicine

    Houston, Texas, United States

  • University of Texas - Houston

    Houston, Texas, United States

  • University of Utah Medical Center

    Salt Lake City, Utah, United States

Site investigator names are published by ClinicalTrials.gov only while a study recruits, so completed studies list sites without them.

Drugs studied

The drug and biological interventions registered on this study, normalized to their RxNorm ingredient where possible.

PlaceboVaginal progesterone
Linked drugs open the directory filtered to KOLs working with them.clinicaltrials.gov ↗

Registration & key dates

Registry attributes as recorded on the ClinicalTrials.gov study record.

Start
13 Nov 2015
Primary completion
15 Dec 2024
Completion
18 Feb 2025
Last update posted
25 Jun 2026
Registered enrollment
1,311
Registry id
NCT02518594

Source: ClinicalTrials.gov, via the CTTI AACT database, data as of 24 Aug 2026. Registry facts are shown as registered by the study sponsor; findmyKOL does not interpret them.