Skip to content

USCOM in Newly Diagnosed FGR Cases

Ultrasound Hemodynamic Assessment in Newly Diagnosed Fetal Growth Restriction: A Pilot Study

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT06343051
Acronym
USCOM FGR
Enrollment
13
Registered
2024-04-02
Start date
2024-07-02
Completion date
2026-05-07
Last updated
2026-08-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fetal Growth Restriction, USCOM

Brief summary

The purpose of this research study is to study the use of an ultrasound measurement system (USCOM) for patients with newly diagnosed fetal growth restriction (FGR). This system uses a technology to measure how much blood is being pumped in and out of the heart, which is important for understanding the heart's function in relation to pregnancy.

Interventions

DEVICEUSCOM

Device that measures how much blood is being pumped in and out of the heart.

Sponsors

Icahn School of Medicine at Mount Sinai
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Pregnant patients with a new diagnosis of fetal growth restriction (estimated fetal weight \<10th percentile or abdominal circumference \<10th percentile) in the third trimester (gestational age \>27w6d)

Exclusion criteria

* Multiple gestation * Fetal anomalies * Gestational diabetes or pregestational diabetes.

Design outcomes

Primary

MeasureTime frameDescription
Systemic vascular resistance obtained from USCOMevery 2-4 weeks at time of prenatal ultrasound, until the end of pregnancyCardiac 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.

Countries

United States

Contacts

STUDY_DIRECTORNicola F Tavella, MPH

Icahn School of Medicine at Mount Sinai

PRINCIPAL_INVESTIGATORRachel J Meislin, MD

Icahn School of Medicine at Mount Sinai

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 25, 2026