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Pregnancies Complicated by Fetal Anomalies (FAR)

University of Tennessee logo

University of Tennessee

Status

Enrolling

Conditions

Congenital Abnormalities
Pregnancy

Study type

Observational

Funder types

Other

Identifiers

NCT02505464
15-03804-XP

Details and patient eligibility

About

The focus of this research is to create a repository of ultrasonographic images and their corresponding medical data from pregnant women (the mothers of the fetuses that are imaged), focusing on fetal anomalies. These women will visit the obstetrical clinics at Regional One Health and the Le Bonheur Fetal Center.

Full description

  1. Repository data will be collected from the medical record and entered into the data base after the patient has completed the appointment.
  2. Data collection will continue into the postpartum period for each participant.
  3. Data collection will continue for the child during the treatment of the medical condition, up to approximately 6 months of age if required by the condition.

Enrollment

500 estimated patients

Sex

All

Ages

1 minute to 50 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • 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 criteria

  • Non-pregnant females.

Trial design

500 participants in 1 patient group

Pregnant Women & their fetuses/infants
Description:
Information about pregnant women and their fetuses/infants, including the medical history, prenatal, perinatal, and postpartum periods (6 weeks after delivery) and throughout the treatment (e.g.surgery) for the child's medical condition (up to approx. child is @ 6 months of age), will be collected in this repository. The analysis of this information may help in understanding of the causes of fetal anomalies.

Trial contacts and locations

5

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Central trial contact

Norman Meyer, M.D.; Annette B. Hickerson, R.N., CCRC

Data sourced from clinicaltrials.gov

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