Clin2
NCT03398629Possibly a fitRecruiting

Study of babies with slow growth or birth defects

Intrauterine Growth RestrictionFetal AnomalyChromosomal AnomaliesPregnancy

Part of Genetic & congenital, Women’s health & pregnancy clinical trials.

This trial looks at how to diagnose and manage pregnancies and babies affected by slow growth before birth, birth defects, or chromosome-related conditions. It may help by improving how doctors confirm problems and plan care for mothers and newborns.

Summary written for real people, not researchers, by Clin2.

Phase
N/A
Enrollment
10,000 people
Ages
Up to 18 years
Study type
Observational

Who can take part

  • You are pregnant (or you are the parent of a newborn/infant) seen at the study hospital
  • Your pregnancy has a prenatal diagnosis of slow growth (IUGR), a structural birth defect, or a chromosome-related issue
  • If a concern is found during pregnancy, it must be confirmed after the baby is born
  • You must agree to join the study
  • The baby must be delivered at the study hospital (not another hospital)

View the official record on ClinicalTrials.gov

Quick eligibility check

Answer a few plain-language questions, based on this study's own requirements, to get a preliminary sense of fit.

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