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NCT Number: NCT07580456

AI for Gastric POCUS ( Point-of-care Ultrasound)

The goal of this observational study is to train and test an AI (Artificial Intelligence)-based program to assist anesthesiologists in the interpretation of stomach ultrasound images and differentiate a "full" from an "empty" stomach.

It is a healthy-volunteer study, where the participants will undergo ultrasound examination of their stomach at three different time points to visualize the stomach contents. These are at fasting state, after taking some solid food and after taking some water. Here, the participants will be randomized to receive one of five different types solid foods and one of five different volumes of water. The stomach ultrasound images will then be used to train and test the accuracy of the model to diagnose the type of stomach content (nothing vs. clear fluid vs. solid food)

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Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Toronto Western Hospital, University Health Network

Toronto, Ontario, M5T 2S8, Canada

Location contact

Anahi Perlas, MD, FRCPC

PRINCIPAL_INVESTIGATOR

Jayanta Chowdhury

CONTACT

[email protected]

4166035800

About this study

Gastric (stomach) Point-of-care ultrasound (POCUS) is an ultrasound examination done at bedside to assess the stomach. It is a validated non-invasive way to find out what is the content in the stomach and its volume. Gastric POCUS is increasingly used before surgery to determine the risk of gastric contents going into the lungs (possibly causing a lung infection and breathing problems) and guide anesthetic management whenever the doctors are not certain about the stomach content based on clinical information.

Gastric POCUS is a relatively new skill for anesthesiologists. While, obtaining the required images is relatively straightforward, the interpretation of such images, however, requires advanced training. Preliminary data have suggested that Artificial Intelligence (AI)-based programs and devices can help in image capturing and its interpretation for other ultrasound applications. This study will be the first to the researcher's knowledge to develop an AI algorithm to enhance anesthesiologists' ability to recognize a full stomach using gastric POCUS. The goal of this observational study is to train and test an AI (Artificial Intelligence)-based program to assist anesthesiologists in the interpretation of stomach ultrasound images and differentiate a "full" from an "empty" stomach.

This is an observational prospective cohort study that follows the CONSORT (Consolidated Standards of Reporting Trials)-AI extension reporting guidelines.

The researchers expect to enroll 30 healthy volunteers for the study.

Following a period of fasting for solids for at least 8 hours and clear fluids for at least 2 hours from the time of study visit. An anesthesiologist or sonographer with a minimum previous experience of 50 gastric ultrasound examinations will perform a standardized gastric ultrasound exam.

A baseline ultrasound examination will be conducted first with the participant lying on their back with the head elevated at 30 degrees (supine position) and then again with the participant lying on their right side (right lateral decubitus position(RLD)).

The same procedure will be repeated twice after ingestion of

  • various volumes of water (100-500) determined at random
  • 1 of 5 different solid or thick fluid foods also determined at random (a banana, an apple, a cup of yogurt, a croissant or a muffin).

Each one of the 30 participants will be randomized to 1 of 5 different volumes of water (100ml, 200ml, 300ml, 400ml, 500ml). Then ultrasound images will be obtained. Subsequently, each participant will also be randomized to 1 of 5 solids (a banana, an apple, a cup of yogurt, a croissant or a muffin) in a 1:1:1:1:1 ratio. A computer-generated list of random numbers for each participant will be created.

The investigators plan to collect 90 10-second clips in total, and each clip can be deconstructed into 10 frozen frames per second, for a total of 100 frozen frames per clip. The investigators expect to generate 9,000 individual images, 80% of which will be used to train the model, 10% to fine-tune and 10% to test the model accuracy. The three de-identified clips from each participant will be normalized and annotated by consultant anesthesiologists to indicate orientation (medial or lateral, cephalad or caudad) and identify relevant structures, as well as the type of content and antral CSA in the right lateral decubitus in case of fluid.

All the collected images will then be fed to an AI to generate computational data.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

A. Inclusion Criteria at the level of the participants

  • Participants must meet all the following inclusion criteria to be eligible for the study:
  • Aged ≥18 years
  • Any sex
  • Be healthy

B. Inclusion Criteria at the level of the input data • Transverse ultrasound images (10 sec clips) of the gastric antrum in the epigastric area that contain all these structures:

  • The edge of the left lobe of the liver
  • The gastric antrum
  • The pancreas
  • The aorta

Exclusion criteria

A. Exclusion Criteria at the level of the participants

  • Participants meeting any of the following exclusion criteria are ineligible for the study:
  • Previous gastro-esophageal surgery (e.g., gastric by-pass, sleeve gastrectomy, fundoplication, partial gastrectomy)
  • Allergy to any of the food that will be provided.

B. Exclusion Criteria at the level of the input data

  • Ultrasound images (10 sec clips) where the gastric antrum cannot be positively identified.

Treatment and study plan

Primary outcomes

  1. To see the overall accuracy of the AI model

    Time frame: Through study completion, an average of 2 years

    To see the overall accuracy of the AI-enhanced ultrasound model to differentiate no content and clear fluid from solid.

Secondary outcomes

  1. To measure the accuracy of the AI model in differentiating a empty from a full stomach

    Time frame: Through study completion, an average of 2 years

    To see the accuracy of the AI-enhanced ultrasound model to differentiate an "empty" (no content or clear fluid with an antral CSA (Cross-sectional Area)< 10 cm2 in the RLD) from a "full" stomach (solid content or clear fluid with an antral CSA > 10cm2 in the RLD).

  2. To measure the balanced accuracy of the AI model

    Time frame: Through study completion, an average of 2 years

    Balanced accuracy accounts for uneven distributions of detected objects (e.g., small vs. large anatomical structures)

  3. To measure the precision of the AI model

    Time frame: Through study completion, an average of 2 years

    Precision evaluates the proportion of true positives among detected objects, addressing false positives that can lead to unnecessary interventions in clinical settings.

  4. To measure the recall of the AI model

    Time frame: Through study completion, an average of 2 years

    (b) Recall (sensitivity) quantifies the model's ability to detect all relevant objects (true positives), critical for avoiding missed detections (false negatives) in important medical diagnoses.

  5. To evaluate the model's classification performance across different confidence thresholds.

    Time frame: Through study completion, an average of 2 years

    Receiver Operating Characteristic (ROC) curves and Area Under Curve (AUC) will be computed to evaluate the model's classification performance across different confidence thresholds.

  6. To evaluate the model's performance in detecting different anatomical structures (e.g., organs, vessels).

    Time frame: Through study completion, an average of 2 years

    Class-specific mean Average Precision (mAP) will be calculated to evaluate the model's performance in detecting different anatomical structures (e.g., organs, vessels). mAP is the standard metric for object detection tasks, summarizing precision and recall across multiple confidence thresholds.

  7. To measure the latency and average inference time per image

    Time frame: Through study completion, an average of 2 years

    Given the clinical need for real-time feedback during ultrasound procedures, the average inference time per image and latency will be measured for each model.

Study contacts

Contact information is provided by the study sponsor or research team.

Jayanta Chowdhury, MBBS,MD

CONTACT

[email protected]

416-603-5800 ext. 2016

Sponsors and collaborators

Lead sponsor

University Health Network, Toronto

Other

Registry information

Official study title

Development of an Artificial Intelligence Algorithm to Enhance the Gastric Point-of-care Ultrasound. A Proof-of-concept Study.

Acronym: POCUS

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
May 12, 2026
Registry last updated
May 12, 2026

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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