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NCT01322529 · ClinicalTrials.gov registry record

Nulliparous Pregnancy Outcomes Study: Monitoring Mothers-to-be

A clinical trial of Pregnancy and Pregnancy Complications, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

Completed
Registry status
10,038
Enrollment target
17
Study locations

NCT01322529: Completed study of Pregnancy and Pregnancy Complications, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

NCT01322529 is a study of Pregnancy and Pregnancy Complications that has completed, run by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD). The registered enrollment target is 10,038 participants, above the 820-participant average among 191 other Pregnancy trials with a reported enrollment target (1124% higher). The trial reports 17 study locations across 8 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01322529, a study of Pregnancy and Pregnancy Complications, has completed, sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD).

COMPLETED
Registry status
10,038 participants
Enrollment target
17
Study locations

Study Summary

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.

Primary Outcome

Delivery of a live born or stillborn infant due to any cause before 37 weeks 0 days project estimated gestational age, after the subject has been enrolled in the study.

Study Locations (17)

Utah

  • McKay Dee Hospital - Ogden
  • Utah Valley Regional Medical Center - Provo
  • University of Utah - Salt Lake City
  • Intermountain Medical Center - Salt Lake City
  • LDS Hospital - Salt Lake City

California

  • Fountain Valley Regional Hospital and Medical Center- UCI MFM private practice - Fountain Valley
  • Long Beach Memorial Medical Center, Women's and Children's Hospital - Women's Perinatal Group, OB Clinic - Long Beach
  • University of California, Irvine, Medical Center - Prenatal care clinics and private practice - Orange

Pennsylvania

  • University of Pennsylvania - Philadelphia
  • West Penn Allegheny Health System - Pittsburgh
  • Magee Womens Hospital - Pittsburgh

Ohio

  • Case Western Reserve University, MetroHealth Medical Center - Cleveland
  • The Ohio State University Medical Center - Columbus

Delaware

  • Christiana Care Health Systems - Newark

Illinois

  • Northwestern University - Chicago

Indiana

  • Indiana University School of Medicine OB/GYN - Indianapolis

New York

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

Trial Details

FieldValue
Enrollment Target 10,038 participants
Start Date 2010-09
Est. Completion 2015-05

What the finished NCT01322529 record still lists

NCT01322529 is an observational study that tracks outcomes without assigning an intervention. Its 10,038 participants enrollment target places it among the larger protocols in the corpus, above the 820-participant average among 191 other Pregnancy trials with a reported enrollment target (1124% higher).

The record links to 2 conditions, with Pregnancy appearing as the primary indexed condition, and to 0 interventions.

NCT01322529 lists 17 locations in 8 states (Utah, California, Pennsylvania).

Frequently Asked Questions

What is clinical trial NCT01322529 about?

NCT01322529 is a clinical study titled "Nulliparous Pregnancy Outcomes Study: Monitoring Mothers-to-be". 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 grou...

What is the current status of trial NCT01322529?

This trial is currently completed. The enrollment target is 10,038 participants. The study started on 2010-09. Estimated completion is 2015-05.

What conditions does trial NCT01322529 study?

This clinical trial studies the following conditions: Pregnancy, Pregnancy Complications.

Who is sponsoring clinical trial NCT01322529?

This trial is sponsored by Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), which has 305 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT01322529 being conducted?

This trial has 17 study locations across California, Delaware, Illinois, Indiana, New York. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Pregnancy

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT01322529's enrollment target sits among peer trials

10,038 4th of 191 higher than 188 of 191 other Pregnancy trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Pregnancy trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT01322529, the US trial registry maintained by the National Library of Medicine. NCT01322529 (large enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.