← Back to Clinical Trials
Recruiting NCT06407388

Ultrasound Findings in Diabetic Pregnancies

Trial Parameters

Condition Diabetes
Sponsor Eastern Virginia Medical School
Study Type OBSERVATIONAL
Phase N/A
Enrollment 156
Sex FEMALE
Min Age 18 Years
Max Age 45 Years
Start Date 2023-06-01
Completion 2025-01-01

Brief Summary

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.

Eligibility Criteria

Inclusion Criteria: * 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 Exclusion Criteria: * 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)

Related Trials