BIOmetric MEasurements in Diagnostics: Comparison of EXperts and IA-assisted Residents
BIOMEDEXIA
1 other identifier
observational
60
1 country
1
Brief Summary
Obstetric ultrasound is the cornerstone of fetal growth assessment. It provides essential biometric measurements for estimating fetal weight, monitoring growth and identifying conditions such as intrauterine growth retardation (IUGR) or macrosomia. The accuracy of these measurements depends largely on the expertise of the operator. Experienced practitioners excel at positioning the probe, identifying anatomical landmarks and obtaining reproducible measurements. In contrast, novice operators, such as medical residents, may find it difficult to capture optimal images or identify precise landmarks, resulting in significant variability. This inter-observer variability, well documented even among experts, can have an impact on clinical decisions and obstetric management. For novices, variability is more pronounced, which can affect diagnostic reliability and patient care. Improving resident training is therefore essential to reduce this variability. Traditional solutions to minimizing variability, such as increased supervision, face limitations due to time constraints and resource availability. Recent advances in Artificial Intelligence (AI) could help in the training of residents. In obstetrics, AI could potentially automate biometric measurements by identifying key anatomical landmarks and performing precise, consistent measurements. These systems might standardize acquisition and reduce variability, making measurements less dependent on operator experience. AI technologies could significantly improve novice performance by potentially shortening the learning curve and enhancing measurement reliability. This might enable residents to work more independently while maintaining accuracy. Despite these potential advantages, few studies would have rigorously compared AI-assisted novice performance with that of expert practitioners under real-world conditions.This study aims to assess the possible effectiveness of AI in supporting novice operators during obstetric biometric measurements. The primary objective would be to determine whether AI assistance could enable novices to achieve measurement accuracy comparable to that of experienced practitioners, while potentially improving reproducibility and reducing inter-observer variability.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at P25-P50 for all trials
Started Apr 2025
1 active site
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Trial Relationships
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Study Timeline
Key milestones and dates
First Submitted
Initial submission to the registry
March 12, 2025
CompletedFirst Posted
Study publicly available on registry
March 24, 2025
CompletedStudy Start
First participant enrolled
April 1, 2025
CompletedPrimary Completion
Last participant's last visit for primary outcome
April 1, 2025
CompletedStudy Completion
Last participant's last visit for all outcomes
April 1, 2025
CompletedApril 25, 2025
March 1, 2025
Same day
March 12, 2025
April 22, 2025
Conditions
Keywords
Outcome Measures
Primary Outcomes (1)
Accuracy of biometric measurements: Assessment of agreement between manual and AI-assisted measurements.
The individual biometric measurements, such as biparietal diameter (BPD), head circumference (HC), abdominal circumference (AC), and femur length (FL), will be presented separately based on their respective units (cm). The estimated fetal weight, which will be based on the aggregation of these various measurements (BPD, HC, AC, FL), will be reported in kilograms (kg). This estimate will be calculated using fetal growth formulas adapted to these parameters. We will clarify that the fetal weight estimate will be calculated based on a model that incorporates these different measurements in the appropriate units. In summary, each measurement will be clearly separated based on its unit, and the fetal weight estimate will be explained to show how the different measurements are combined.
36 weeks amenorrhea
Study Arms (1)
Routine Follow-Up: Patients scheduled for a standard biometric ultrasound.
Maternal Age: Pregnant women aged between 18 and 45 years. Pregnancy Type: Singleton viable pregnancy (excluding twin or multiple gestations). Gestational Age: Between 17 weeks and 38 weeks of gestation.
Interventions
In this study, biometric measurements were systematically performed for each patient using both manual methods and an artificial intelligence (AI) system (Live View Assist, Samsung). The AI system provided real-time guidance by identifying anatomical landmarks and assisting in the measurement of key biometric parameters, including Femur Length (FL), Abdominal Circumference (AC), Head Circumference (HC), and Biparietal Diameter (BPD). This dual approach ensured that both manual and AI-assisted methods were applied uniformly as part of routine clinical care.
Eligibility Criteria
Pregnant woman
You may qualify if:
- Pregnant women aged between 18 and 40 years.
- Singleton or twin ongoing pregnancies.
- Gestational age between 20 and 36 weeks of amenorrhea (WA).
- Patients scheduled for a biometric ultrasound (standard follow-up).
You may not qualify if:
- Known major fetal anomalies that could affect biometric measurements.
- Technical difficulties during the ultrasound (e.g., maternal obesity, complex abdominal scars).
- History of severe maternal conditions affecting biometric measurements (e.g., uterine malformations)
Contact the study team to confirm eligibility.
Sponsors & Collaborators
Study Sites (1)
Hospices Civils de Lyon, Maternité Croix Rousse
Lyon, 69004, France
Study Design
- Study Type
- observational
- Observational Model
- COHORT
- Time Perspective
- RETROSPECTIVE
- Sponsor Type
- OTHER
- Responsible Party
- SPONSOR
Study Record Dates
First Submitted
March 12, 2025
First Posted
March 24, 2025
Study Start
April 1, 2025
Primary Completion
April 1, 2025
Study Completion
April 1, 2025
Last Updated
April 25, 2025
Record last verified: 2025-03