MRI Assessment of Placental Health

Recruiting Observational Study
Intrauterine Growth Restriction
No Placebo Group Every participant receives an active treatment — no one gets a placebo. Healthy Volunteers Welcome You do not need to have the condition being studied to take part. No Study Drug Researchers observe your health over time — no experimental treatment is given.
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At a Glance
Age
18 – 45
Sex
Female
Study type
Observational
Participants needed
80 (estimated)
Sponsor
Boston Children's Hospital · Other
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About This Trial
The ultimate goal of this project is to develop methods that allow informed decision-making on the delivery time of fetuses that are at increased risk of stillbirth due to IUGR. In placenta related IUGR pregnancies, there can be multiple concurrent placental pathologies. Although there is no specific correspondence between a single type of pathology and IUGR, the common result of these pathologies…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: 1. The pregnant mother with twin gestation with diagnosis of selective IUGR based upon obstetrical US findings as following: * Proven monochorionicity / dichorionicity * Discordance in estimated fetal weight (EFW). Growth restriction (\<10 percentile of norm) in one or bo…
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