USCOM in Newly Diagnosed FGR Cases

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

RECRUITING

Total Enrollment

100 participants

Study Classification

OBSERVATIONAL

Study Start Date

2024-07-02

Study Completion Date

2026-06-30

Brief Summary

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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.

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Detailed Description

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Conditions

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Fetal Growth Restriction USCOM

Study Design

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Observational Model Type

COHORT

Study Time Perspective

PROSPECTIVE

Study Groups

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Fetal Growth Restriction diagnosed > 27w6d gestation

Patients with a new diagnosis of fetal growth restriction after 27 weeks 6 days' gestation.

USCOM

Intervention Type DEVICE

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

Interventions

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USCOM

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

Intervention Type DEVICE

Eligibility Criteria

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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)