Pregnancies Complicated by Fetal Anomalies
Purpose
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.
Conditions
- Pregnancy
- Congenital Abnormalities
Eligibility
- Eligible Ages
- Between 1 Minute and 50 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
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.
Study Design
- Phase
- Study Type
- Observational [Patient Registry]
- Observational Model
- Case-Only
- Time Perspective
- Prospective
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
| Pregnant Women & their fetuses/infants | 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. |
Recruiting Locations
LeBonheur Children's Hospital
Memphis, Tennessee 38103
Memphis, Tennessee 38103
Methodist LeBonheur Healthcare, LeBonheur Fetal Center
Memphis, Tennessee 38103
Memphis, Tennessee 38103
Regional One Health, OB/GYN Clinic, Maternal Fetal Medicine
Memphis, Tennessee 38103
Memphis, Tennessee 38103
Regional One Health, Regional Medical Center, Rout Center for Women and Children
Memphis, Tennessee 38103
Memphis, Tennessee 38103
Regional One Health Center for High Risk Pregnancies
Memphis, Tennessee 38120
Memphis, Tennessee 38120
More Details
- Status
- Recruiting
- Sponsor
- University of Tennessee
Detailed 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.