USCOM for Fetal Growth Restriction (FGR)
This study is looking at how a device called USCOM can be used in pregnant patients who have recently been diagnosed with Fetal Growth Restriction (FGR). FGR means the baby is not growing as expected. The USCOM device measures how much blood is being pumped in and out of the heart. Researchers want to see if this measurement, called systemic vascular resistance, can help them understand the heart's function during pregnancy in these cases. You might be able to join if you are pregnant, at least 18 years old, and have a new diagnosis of FGR in your third trimester (after 27 weeks and 6 days of pregnancy). The study is currently unclear on its recruitment status and plans to enroll 100 participants.
- Study design
- This is an observational study, meaning researchers will be watching and collecting information. It plans to include 100 participants.
- What's involved
- You would have your systemic vascular resistance measured using the USCOM device every 2-4 weeks during your prenatal ultrasounds, until the end of your pregnancy.
- Compensation
- Not stated in the trial record.
- Follow-up
- Measurements will be taken until the end of your pregnancy.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
USCOM in Newly Diagnosed FGR Cases
At a glance
Conditions
Where it's being run
1 sites across 1 statesStudy leadership
- Nicola F Tavella, MPH · STUDY_DIRECTOR · Icahn School of Medicine at Mount Sinai
- Rachel J Meislin, MD · PRINCIPAL_INVESTIGATOR · Icahn School of Medicine at Mount Sinai
Who to contact
This trial hasn't published a contact. View it on ClinicalTrials.gov
Do you actually qualify for this trial?
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Inclusion
Exclusion
What this trial measures
- Systemic vascular resistance obtained from USCOMevery 2-4 weeks at time of prenatal ultrasound, until the end of pregnancy
Cardiac output related to systemic vascular resistance (SVR) obtained from the USCOM device. SVR is an indicator of general resistance experienced within the circulatory system and is correlated with an array of cardiac related adverse health outcomes. The USCOM device uses noninvasive ultrasonographic technology to determine SVR at the time of prenatal ultrasound.