Pregnancies Complicated by Fetal Anomalies
For patients and families
In plain language
An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.
- What is being studied
- This is an observational study: the protocol does not assign a study treatment.
- Who it may be relevant to
- Registry conditions: Pregnancy, Congenital Abnormalities. Basic parameters: 1 Minute — 50 years · All.
- What needs checking
- Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
- Where it takes place
- United States
- Next step
- Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Unsure about the terms? Read our patient guide →
Official title
Characteristics of Pregnancies Complicated by Fetal Anomalies
Overview
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.
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.
Primary outcome measures
- Data Collection [Time frame: From the initial visit @ the High Risk Clinic through the infants approx. age of 6 months]
Eligibility criteria
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.
Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.
Healthy volunteers: No
Study design
- Observational model
- Case-only
Study locations
United States · 5 centers
- LeBonheur Children's Hospital — Memphis
- Methodist LeBonheur Healthcare, LeBonheur Fetal Center — Memphis
- Regional One Health, OB/GYN Clinic, Maternal Fetal Medicine — Memphis
- Regional One Health, Regional Medical Center, Rout Center for Women and Children — Memphis
- Regional One Health Center for High Risk Pregnancies — Memphis
Identifiers
NCT: NCT02505464 · 15-03804-XP