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NCT Number: NCT07414446

Non-Invasive Detection of Pulmonary Right-to-Left Shunts Using the SONAS Ultrasound Device

The goal of this clinical trial is to learn how well the SONAS ultrasound device can detect right-to-left shunts of adults with hereditary hemorrhagic telangiectasia (HHT) who are already scheduled for a contrast bubble echocardiogram (TTCE). The main questions it aims to answer are:

1. How accurately does SONAS detect right-to-left shunts compared to the standard TTCE test? 2. Can SONAS results help tell the difference between shunts in the heart and shunts in the lungs?

Participants will wear a headband with the SONAS device on the head while they undergo their routine TTCE bubble test. They will receive the usual contrast (agitated saline) through a vein, and both SONAS and TTCE signals will be recorded at the same time. There will be one examination in rest, and one during a breathing exercise (the Valsalva manoeuvre).

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Key information

About this study

This study is being done to find out whether a new ultrasound device called SONAS can safely and reliably detect "right-to-left shunts" in people with hereditary hemorrhagic telangiectasia (HHT). Right-to-left shunts are abnormal connections between blood vessels that allow blood to bypass the lungs and go directly from the right side of the heart to the left side. This can increase the risk of problems such as stroke or brain abscess. Today, these shunts are usually found with a "bubble heart ultrasound" (TTCE), which needs experienced staff and can be time-consuming. SONAS is a small, portable device that detects blood flow signals in the brain after a bubble injection and may offer a simpler way to detect these shunts.

In this study, all participants are are already scheduled to have a bubble heart ultrasound as part of their regular care. The study adds the SONAS device on top of this routine test. During the procedure, a soft headband with small ultrasound sensors is placed in frond of the ears on both sides of the head. At the same time, the standard bubble test is done: normal saline mixed with a small amount of the participant's blood and some air is injected into a vein, and the heart is imaged with ultrasound. Participants will be asked to perform a straining manoeuvre (called a Valsalva) to see if this makes a shunt more visible. While this is happening, SONAS continuously records signals from the brain that show when the bubbles pass through.

There will be a comparison between what SONAS shows with what the standard heart ultrasound shows. By comparing these results, the researchers want to see how closely the SONAS score matches the standard test and whether certain SONAS outcomes indicate a clinically important shunt. They will also look at the timing and pattern of the bubble signals to explore whether SONAS can help tell the difference between shunts that come from the heart and those that come from the lungs. The study does not change any decisions about diagnosis or treatment: all medical decisions remain based on the usual heart ultrasound and other standard tests.

Throughout the procedure, the safety and comfort of participants are closely monitored. SONAS does not deliver any contrast or radiation. All problems or unusual events that occur during or shortly after the combined test are recorded. The information collected in this study will help determine whether SONAS is a practical, safe, and useful tool to support or simplify screening for right-to-left shunts.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Age 18 years or older.
  • Suspected or confirmed hereditary hemorrhagic telangiectasia (HHT).
  • Incidentally: Patients who have experienced cryptogenic stroke

Exclusion criteria

  • Pregnancy or breastfeeding.
  • Known or suspected fracture(s) of the temporal / parietal skull bones, or with open skin injuries in the anatomical area of the temporal / parietal lobes.
  • Patients with known metal skull implants in the anatomical area of the temporal / parietal bones, or with anatomical formation of the head or ear tha may interfere with proper headset placement.
  • Patients with known allergies or reactions to parabens, which are present in the gel pad material of the applied part.

Treatment and study plan

Transcranial Ultrasound Device

Device

The intervention is the SONAS ultrasound device used during a routine bubble echocardiogram. A battery-powered unit connects to a headset with two ultrasound sensors placed in front of the ears. The device does not deliver contrast or drugs; it records ultrasound signals in the brain while standard agitated saline is injected and the heart is imaged. SONAS analyzes bubble-related signals and calculates a numeric score to evaluate right-to-left shunts without changing the usual echocardiography protocol.

Other names: SONAS, Foqus

Primary outcomes

  1. Capability of detecting Right-to-Left Shunts

    Time frame: Periprocedurally

    Device capability of detecting High Intensity Transient Signals (HITS) using SONAS in presence of RLS, as confirmed by reference method TTCE. SONAS output is expressed as maximum HITS Density Score (0-100%). TTCE outcome is assessed by RLS grade (0-3), maximum microbubble count in left ventricle, and corrected change in echo density.

  2. Diagnostic accuracy

    Time frame: Periprocedurally

    Diagnostic accuracy (sensitivity and specificity) of SONAS for detection of clinically significant RLS (≥grade 2 on TTCE) at different HITS Density Score thresholds.

Secondary outcomes

  1. Distinguishing intracardiac from pulmonary Right-to-Left Shunts

    Time frame: Periprocedurally

    SONAS capability to distinguish intracardiac from pulmonary RLS based on time delay between contrast administration and first HITS occurrence, and difference in HITS Density Score between rest and Valsalva maneuver.

  2. Test-retest reliability of SONAS for HITS assessment

    Time frame: Periprocedurally

    Test-retest reliability of SONAS for HITS assessment using Intraclass Correlation Coefficient.

Study contacts

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

Pier HJ van Veen, Medical Doctor

CONTACT

[email protected]

0883205336

Sponsors and collaborators

Lead sponsor

St. Antonius Hospital

Other

Collaborators

  • Burl Concepts, Inc.

Registry information

Official study title

Novel Approach For The Non-Invasive Detection of Pulmonary Right-to-Left Shunts

Acronym: SONAS

Important dates

Study start
2026
Primary completion
2026
Study completion
2026
First posted
Feb 17, 2026
Registry last updated
Feb 17, 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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