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Diagnostic Ultrasound System for Obstetric Imaging

This study is testing a new Diagnostic Ultrasound System called UIH uSONIQUE Nova. The goal is to collect high-quality ultrasound images of babies during pregnancy. These images will help develop and improve artificial intelligence (AI) tools that can automatically measure parts of the baby. This research will help the company get approval from the U.S. FDA for this new ultrasound system. You may be able to join if you are a pregnant woman between 18 and 45 years old, have one baby, and are 18 to 28 weeks pregnant. The study aims to collect a complete set of fetal biometric images. The current status of this study is unclear.

Study design
This is an observational study planning to enroll 50 pregnant participants.
What's involved
You would have an obstetric ultrasound using the investigational diagnostic ultrasound system to perform a fetal anatomic survey of your abdomen.
Compensation
Not stated in the trial record.
Follow-up
The primary endpoint, collecting fetal biometric images, is measured at Day 1.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT07590063

Technology Development of Diagnostic Ultrasound System for Obstetric Imaging

Not Yet Recruiting
Not specifiedAges 18–45Observational
United Imaging Healthcare North America, Inc.
~50 participants
Updated 2026-05-15 on ClinicalTrials.gov
What's tested:Diagnostic Ultrasound System

At a glance

Recruiting sites
0 of 1 listed site is recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Complete Fetal Biometric Image Set Collection
Measured over Day 1

Conditions

Pregnancy

Explore related trials

Pregnancy

Where it's being run

1 sites across 1 states
Oregon1

Who to contact

Adam Principal Investigator, MD, MPH
[email protected]
503-494-6852
Email the study team

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Do you actually qualify for this trial?

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Eligibility criteria

Exclusion

Body Mass Index (BMI) \> 40
Prior surgeries including: abdominal mesh placement; abdominoplasty
Vaginal bleeding within the last 6 weeks 4. Patients with serious medical comorbidities including: maternal congenital heart abnormalities; history of organ transplant; asthma exacerbation (during pregnancy); pre-eclampsia; recent mechanical trauma. 5. Use of any of the following during pregnancy: marijuana (or similar derivatives); alcohol; tobacco; methamphetamines; warfarin; isotretinoin; methotrexate; valproic acid; retinoids; oral steroids 6. Non-English speaking. 7. Participants deemed unsuitable by the investigator due to safety or data integrity.

What this trial measures

  • Complete Fetal Biometric Image Set CollectionDay 1

    Number of participants from whom complete fetal biometric image sets are successfully collected, including Biparietal Diameter (BPD), Head Circumference (HC), Abdominal Circumference (AC), and Femur Length (FL), in compliance with the study scanning protocol standards