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Clinical trialNCT01322529CompletedObservational

Nulliparous Pregnancy Outcomes Study: Monitoring Mothers-to-be

SponsorEunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD)Enrollment10,038PregnancyPregnancy Complications
View the registry record on ClinicalTrials.gov

Summary

The lay summary the sponsor registered on ClinicalTrials.gov.

Forty percent of pregnant women in the United States are women who have never given birth. As a group, they sometimes have complications with their pregnancy, but there is no information from a previous pregnancy to identify who might have a problem. Very little research has been done with this group. The Nulliparous Pregnancy Outcomes Study: Monitoring Mothers-to-be (nuMoM2b) is collecting data from a diverse population of about 10,000 women who are having their first baby and are carrying only one baby. The women are enrolled early in pregnancy and undergo research assessments four times during their pregnancies. Data are collected through interviews, self-completed data forms, clinical measurements, ultrasound, and collection and storage of blood samples, urine samples, and fluid from the vagina and cervix. Some information comes from medical records. A subset of women may be asked to participate in substudies collecting information on sleep breathing, sleep patterns and quality, or other areas possibly related to birth outcomes. The goal of the research is to find ways to identify women in this group who might develop a problem with their pregnancy and use this information to improve the health of pregnant women and their babies in the future. The study is focusing on pregnancy problems like high blood pressure, babies that are born much too early and very small babies.

Investigators

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

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

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

United States
  • Fountain Valley Regional Hospital and Medical Center- Uci Mfm Private Practice

    Fountain Valley, California, United States

  • Long Beach Memorial Medical Center, Women'S and Children'S Hospital - Women'S Perinatal Group, Ob Clinic

    Long Beach, California, United States

  • University of California, Irvine, Medical Center - Prenatal Care Clinics and Private Practice

    Orange, California, United States

  • Christiana Care Health Systems

    Newark, Delaware, United States

  • Northwestern University

    Chicago, Illinois, United States

  • Indiana University School of Medicine Ob/gyn

    Indianapolis, Indiana, United States

  • Columbia University Medical Center- Department of Obstetrics and Gynecology Division of Maternal Fetal Medicine

    New York, New York, United States

  • Case Western Reserve University, Metrohealth Medical Center

    Cleveland, Ohio, United States

  • the Ohio State University Medical Center

    Columbus, Ohio, United States

  • University of Pennsylvania

    Philadelphia, Pennsylvania, United States

  • Magee Womens Hospital

    Pittsburgh, Pennsylvania, United States

  • West Penn Allegheny Health System

    Pittsburgh, Pennsylvania, United States

  • Mckay Dee Hospital

    Ogden, Utah, United States

  • Utah Valley Regional Medical Center

    Provo, Utah, United States

  • Intermountain Medical Center

    Salt Lake City, Utah, United States

  • Lds Hospital

    Salt Lake City, Utah, United States

  • University of Utah

    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

No drug or biological interventions are in our data for this study. It may test a procedure, device or behavioral intervention, or the intervention list isn't in our current snapshot. See the registry record ↗. Why? →

Registration & key dates

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

Start
30 Sept 2010
Primary completion
31 May 2015
Completion
31 May 2015
Last update posted
12 Jan 2016
Registered enrollment
10,038
Registry id
NCT01322529

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.