Generic Database of Very Low Birth Weight Infants

NCT00063063 · Status: RECRUITING · Type: OBSERVATIONAL · Enrollment: 80000

Last updated 2026-03-16

No results posted yet for this study

Summary

The Generic Database (GDB) is a registry of very low birth weight infants born alive in NICHD Neonatal Research Network (NRN) centers. The GDB collects observational baseline data on both mothers and infants, and the therapies used and outcomes of the infants. The information collected is not specific to a disease or treatment (i.e., it is "generic"). Data are analyzed to find associations and trends between baseline information, treatments, and infant outcome, and to develop future NRN trials.

Conditions

  • Infant, Newborn
  • Infant, Low Birth Weight
  • Infant, Small for Gestational Age
  • Infant, Premature

Interventions

OTHER

No Intervention

Sponsors & Collaborators

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

    collaborator NIH
  • NICHD Neonatal Research Network

    lead NETWORK

Principal Investigators

  • Abbot R Laptook, MD · Brown University, Women & Infants Hospital of Rhode Island

  • Anna Maria Hibbs, MD, MSCE, FAAP · Case Western Reserve University, Rainbow Babies and Children's Hospital

  • C. Michael Cotten, MD · Duke University

  • Ravi M Patel, MD, MSc · Emory University

  • Abhik Das, PhD · RTI International

  • Krisa P Van Meurs, MD · Stanford University

  • Stephanie Merhar, MD MS · Children's Hospital Medical Center, Cincinnati

  • Waldemar A Carlo, MD · University of Alabama at Birmingham

  • Tarah Colaizy, MD, MPH · University of Iowa

  • Kristi L Watterberg, MD · University of New Mexico

  • Myra Wyckoff, MD · University of Texas, Southwestern Medical Center at Dallas

  • Jon E Tyson, MD MPH · The University of Texas Health Science Center, Houston

  • Sara DeMauro, MD, MSCE · University of Pennsylvania

  • Carl D'Angio, MD · University of Rochester

  • Pablo Sanchez, MD · Research Institute at Nationwide Children's Hospital

  • Robin Ohls, MD · University of Utah

Eligibility

Max Age
14 Days
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
1987-04-01
Primary Completion
2030-03-31
Completion
2030-03-31

Countries

  • United States

Study Locations

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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 NCT00063063 on ClinicalTrials.gov