Observational Study of Pregnancies with Fetal Anomalies

This is an observational study focused on understanding pregnancies complicated by fetal anomalies (birth defects). Researchers are creating a collection of ultrasound images and medical information from pregnant women who visit high-risk pregnancy clinics. They are also collecting data from infants born with anomalies. The goal is to gather information from the initial clinic visit through the infant's first six months of life. You may be able to join if you are a pregnant female, aged 8 to 50, referred to a high-risk pregnancy clinic, or if you have an infant born with anomalies. This study is collecting data, not testing a specific drug or intervention. The current recruitment status is unclear.

Study design
This is an observational study with a planned enrollment of 500 participants. It is not testing a specific intervention.
What's involved
Data will be collected from your medical record after your appointment and will continue into the postpartum period. For your child, data collection will continue during treatment up to approximately 6 months of age.
Compensation
Not stated in the trial record.
Follow-up
Data collection will continue through the infant's approximate age of 6 months.

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NCT02505464

Pregnancies Complicated by Fetal Anomalies

Recruiting
Not specifiedAges 1–50Observational
University of Tennessee
~500 participants
Updated 2024-12-09 on ClinicalTrials.gov

At a glance

Recruiting sites
5 of 5 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Data Collection
Measured over From the initial visit @ the High Risk Clinic through the infants approx. age of 6 months
Pregnancy
Congenital Abnormalities
5 sites across 1 states
Tennessee5
  • Norman Meyer, M.D. · PRINCIPAL_INVESTIGATOR · Vice-Chair and Professor, MFM Fellowship Director Obstetrics and Gynecology

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Eligibility criteria

Inclusion

Pregnant females
age 8 years to 50 years
who have referred to the clinic for high risks pregnancies
Infants (male and female) born with anomalies

Exclusion

Non-pregnant females.
  • Data CollectionFrom the initial visit @ the High Risk Clinic through the infants approx. age of 6 months

    Data collection from participant's medical records will be entered into a data base