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Limiting Adverse Birth Outcomes in Resource-Limited Settings

NCT04102644 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 12020

Last updated 2022-09-27

No results posted yet for this study

Summary

The primary objective of this research is to exhaustively document the course and outcomes of hospitalization, labor, delivery, and early postpartum course of up to 15,000 mother-newborn pairs in settings where the occurrence of adverse outcomes is high. The Investigators will gather detailed laboratory, physiologic, and clinical information, and precisely characterize major adverse diagnoses and outcomes. The resulting high-quality, granular, and generalizable data will be used to develop new algorithms to signal actionable intrapartum diagnoses and prospectively stratify women according to their risk for adverse maternal and neonatal outcomes.

Conditions

  • Birth Outcomes
  • Labor and Delivery
  • Respiratory Infection

Interventions

OTHER

Observation

Documentation of course and outcome of hospitalization, labor, delivery, and postpartum period

Sponsors & Collaborators

  • Bill and Melinda Gates Foundation

    collaborator OTHER

  • University of North Carolina, Chapel Hill

    lead OTHER

Principal Investigators

  • Jeff Stringer, MD, FACOG · University of North Carolina, Chapel Hill

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2019-10-31
Primary Completion
2022-08-08
Completion
2022-09-20

Countries

  • Ghana
  • India
  • Zambia

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 NCT04102644 on ClinicalTrials.gov