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Maternal Newborn Health Registry

Global Network for Women's and Children's Health Research Maternal Newborn Health Registry

Who can join

All ages · All sexes · Healthy volunteers welcome

Inclusion Criteria:

* Community-level

  * Appropriate for long-term registry data collection and the conduct of ongoing Global Network research
  * At least 300 deliveries per year
* Participant-level

  * Pregnant women intending to deliver within study cluster
  * Women who deliver within the study cluster
  * Women who reside in the community but are transferred for care at delivery

Exclusion Criteria:

* Participant-level

  * Opt out of consent to include data in the study

About the study

The primary purpose of this population-based study is to quantify and understand the trends in pregnancy outcomes in defined low-resource geographic areas over time, in order to provide population-based data on stillbirths, neonatal and maternal mortality.

What is being tested

• There is no intervention associated with the parent MNHR study. For the MNHR COVID sub-study, participants will be asked to provide a blood specimen at or near delivery. (other)

Sponsor: NICHD Global Network for Women's and Children's Health · Participants: 950,000 · Started: 2008-05

Contact the study team

• Marion Koso-Thomas, MD · Phone: 301-435-6873
• Elizabeth McClure, PHD · Phone: 919-316-3773

Official record on ClinicalTrials.gov — NCT01073475

Locations in the U.S.

Conditions

• Maternal Death
• Stillbirth

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.