RECRUITING

Ultrasound Findings in Diabetic Pregnancies

Conditions

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

Description

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.

Official Title

Ultrasound Findings Predictive of Neonatal Outcomes in Diabetic Pregnancies

Quick Facts

Study Start:2023-06-01
Study Completion:2025-06-01
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:RECRUITING

Study ID

NCT06407388

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

Ages Eligible for Study:18 Years to 45 Years
Sexes Eligible for Study:FEMALE
Accepts Healthy Volunteers:No
Standard Ages:ADULT
Inclusion CriteriaExclusion Criteria
  1. * Patients who enter pregnancy with a diagnosis of type I or type II diabetes mellitus.
  2. * Pregnant women between the ages of 18-45
  3. * Live, singleton gestation
  4. * Understanding and ability to give informed consent
  1. * Patient unwilling or unable to provide consent
  2. * Intrauterine fetal demise (no fetal heart beat identified and documented by two physicians)
  3. * Age less than 18 years of age
  4. * Multifetal gestation
  5. * Chromosomal abnormality
  6. * Congenital infection (Toxoplasmosis, Cytomegalovirus, Rubella, Varicella Zoster, Parvovirus B19
  7. * Major fetal congenital malformations (such as: major congenital heart defect, omphalocele, open neural tube defect, etc)

Contacts and Locations

Study Contact

Kristin Ayers, MPH
CONTACT
7574460579
ayerskl@evms.edu

Study Locations (Sites)

Department of Obstetrics and Gynecology, Division of Maternal-Fetal Medicine, Eastern Virginia Medical School
Norfolk, Virginia, 23507
United States

Collaborators and Investigators

Sponsor: Eastern Virginia Medical School

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2023-06-01
Study Completion Date2025-06-01

Study Record Updates

Study Start Date2023-06-01
Study Completion Date2025-06-01

Terms related to this study

Additional Relevant MeSH Terms

  • Diabetes