Pregnancies Complicated by Fetal Anomalies
Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age1-50
SponsorUniversity of Tennessee
About this trial
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.
Eligibility criteria
This trial does not accept healthy volunteersQualifiers
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
Disqualifiers
Non-pregnant females.
Trial population
All patients referred to, or being seen in the Ob-Gyn High Risk Clinics (ROH-MFM Clinic, ROH-CHRP, ROH-Rout Center, Le Bonheur Fetal Center) will be potential participants.
Trial design
Design model
Case-only
Time perspective
Prospective
Treatments tested in this trial
Not listed
Trial groups
500 Participants
are grouped into 1 trial groupGroup A: Pregnant Women & their fetuses/infants
Trial outcomes
Primary outcomes
1
Data Collection
Data collection from participant's medical records will be entered into a data base
Time frame
From the initial visit @ the High Risk Clinic through the infants approx. age of 6 monthsSponsors and contacts
Click on the lead sponsor to view all of their trials.
University of Tennessee
Lead sponsor
Regional One Health
Collaborator
Source ClinicalTrials.gov