Actively Recruiting
Ultrasound Findings in Diabetic Pregnancies
Led by Eastern Virginia Medical School · Updated on 2024-05-09
156
Participants Needed
1
Research Sites
104 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
The goal of our study is to identify ultrasonographic markers that can predict adverse neonatal outcomes. Specifically, we hypothesize that an increase in fetal liver volumes will increase transcutaneous bilirubin (TcB) in the newborn and thus jaundice requiring phototherapy. This information can be used in patient counseling and to guide future screening protocols for ultrasound in individuals with diabetes.
CONDITIONS
Official Title
Ultrasound Findings in Diabetic Pregnancies
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients who enter pregnancy with a diagnosis of type I or type II diabetes mellitus.
- Pregnant women between the ages of 18-45
- Live, singleton gestation
- Understanding and ability to give informed consent
You will not qualify if you...
- Patient unwilling or unable to provide consent
- Intrauterine fetal demise (no fetal heart beat identified and documented by two physicians)
- Age less than 18 years of age
- Multifetal gestation
- Chromosomal abnormality
- Congenital infection (Toxoplasmosis, Cytomegalovirus, Rubella, Varicella Zoster, Parvovirus B19
- Major fetal congenital malformations (such as: major congenital heart defect, omphalocele, open neural tube defect, etc)
AI-Screening
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Trial Site Locations
Total: 1 location
1
Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Eastern Virginia Medical School
Norfolk, Virginia, United States, 23507
Actively Recruiting
Research Team
K
Kristin Ayers, MPH
CONTACT
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
2
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