Skip to main content
OpenTrials
Completed

NCT Number: NCT06652568

Determining the Validity of ThinkSono Guidance for Ultrasound Image Acquisition and Remote Detection

The purpose of this study is to confirm the safety and efficacy of ThinkSono Guidance, a software data collection and communication tool designed to collect ultrasound data to help detect blood clots in veins. The ThinkSono system is CE Mark approved in the European Union and in clinical use in Europe. Usually, when an ultrasound is conducted to detect blood clots in veins, a sonographer (trained technologist who conducts ultrasounds) and/or radiologist will conduct the procedure, including a compression ultrasound exam, and the scan may require a bulky cart and ultrasound equipment. ThinkSono Guidance is a mobile software application that enables other healthcare professionals such as nurses, non-radiologist physicians including general practitioners, and other allied healthcare professionals to perform the ultrasound at the point of care using guidance from the software app. This is a multi-site non-randomized, double-blinded, prospective cohort pivotal study.

Completed

Looking for future studies?

Notify Me

Key information

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Primary location

NYU Langone Health, New York, United States

Loading trial locations.

About this study

Deep vein thrombosis (DVT) is well recognized to cause significant morbidity and mortality both at the time of diagnosis and post-diagnosis. With an estimated incidence of 1- 2 per 1,000 people, over to 300,000 people in the US will be diagnosed with venous thromboembolism (VTE) per annum and two-thirds of these will be DVT. However, positive cases only represent 12-25% of the total number of patients who present with suspected DVT. In other words, between 75-88% of suspected DVT cases, when fully investigated, are negative. Estimates have placed the yearly cost of VTE to the US healthcare system at up to $10 billion.

It is notoriously difficult to diagnose a DVT by clinical acumen alone. The standard approach to making a diagnosis of proximal DVT currently involves an algorithm combining pre-test probability assessment through the Wells score, and compression ultrasonography. Handheld ultrasound probes have recently become available. These probes have enabled 'app-based' compression ultrasonography to be performed without the need for bulky cart or laptop-based ultrasound machines. These new machines have a small form factor, meaning only the ultrasound probe is required for diagnostic purposes in conjunction with a smartphone or tablet.

At present, although the new handheld probes are smaller and are better suited for point of care diagnosis, they still require an experienced radiologist or sonographer to perform the compression exam. This means that these devices can only be used wherever sonographers/radiologists are based most often i.e. hospital radiology departments. However, due to recent advances in "machine learning", software is now being developed for these 'app-based' probes that can assist non-radiology specialist healthcare professionals (e.g. nurses, non-radiologist physicians, general practitioners and other allied healthcare professionals) to carry out the compression ultrasound exam with minimal training.

ThinkSono Guidance is a guidance software expected to help non-radiology specialist healthcare professionals produce compression ultrasound image data that meet or exceed the minimal image quality criteria for a remote diagnosis by an expert (e.g. radiologist). The ThinkSono system is CE Mark approved in the European Union and in clinical use in Europe.

This study is a multi-site non-randomized, double-blinded, prospective cohort pivotal study. The purpose of this study is to confirm the safety and efficacy of ThinkSono Guidance as per the intended use defined as:

ThinkSono Guidance is a guidance, data acquisition and communication tool that guides non-ultrasound-trained healthcare staff to collect point of care compression ultrasound data in the proximal deep venous system of the lower extremity for interpretation by qualified clinicians.

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • The participant is willing to provide written informed consent to participate in this research.
  • The participant is over the age of 18
  • The participant has symptoms suggestive of a deep venous thrombosis (DVT)
  • The diagnostic DVT algorithm indicates that an ultrasound is needed

Exclusion criteria

  • Patient consent not given or retracted during the study.
  • Local imaging specialists fail to scan the patient or fail to produce a conclusive imaging diagnosis.
  • Incomplete ThinkSono Guidance scan due to logistical or other issues such as pain, lack of patient cooperation, barriers such as a cast or other physical limitations.
  • Pregnant women
  • Patients who undergo a local imaging scan and initiation of new treatment for DVT (e.g. lytic agents, therapeutic anticoagulation, or intervention after the local imaging scan) before a ThinkSono scan can be performed.

Treatment and study plan

ThinkSono System

Device

The ThinkSono Guidance System is a guidance software expected to help non-radiology specialist healthcare professionals produce compression ultrasound image data that meet or exceed the minimal image quality criteria for a remote diagnosis by an expert (e.g. radiologist).

Primary outcomes

  1. Image Quality Adequacy

    Time frame: Measured during ThinkSono Guidance scanning (median scan time of 5.4 minutes).

    ThinkSono Guidance achieves adequate image quality with an American College of Emergency Physicians (ACEP) score equal to or greater than 3 in at least 60% of scans to show that non-ultrasound-trained operators can acquire relevant cine-loops (an expectation ≥75%, lower CI ≥60%). The ACEP score is a score on a scale of 1-5 assessing utilized as the national standard for image quality evaluation. Further information is available at: https://www.acep.org/siteassets/uploads/uploaded-files/acep/clinical-and-practice-management/policy-statements/information-papers/emergency-ultrasound-standard-reporting-guidelines---2018.pdf.

Secondary outcomes

  1. Triage Sensitivity

    Time frame: Measured during ThinkSono Guidance scanning (median scan time of 5.4 minutes).

    The sensitivity for overall triage performance for proximal DVT is at least 85%.

  2. Triage Specificity

    Time frame: Measured during ThinkSono Guidance scanning (median scan time of 5.4 minutes).

    The specificity for overall triage performance for proximal DVT is at least 30%.

  3. Prioritization Specificity

    Time frame: Measured during ThinkSono Guidance scanning (median scan time of 5.4 minutes).

    Prioritization specificity quantifies how reliably the system identifies patients who merit high-urgency imaging specialist assessment based on their ThinkSono scans. A high prioritization specificity means that there are very few false-positive scans that lead to patients being prioritized unnecessarily. Further details are available in the trial protocol and statistical analysis plan.

    ThinkSono Guidance achieves specificity for prioritizing patients of at least 93%. This means that at least 93% of scans without proximal lower extremity DVT were not labeled as false positives by reviewers of ThinkSono Guidance scans.

  4. Predictive Values

    Time frame: Measured during ThinkSono Guidance scanning (median scan time of 5.4 minutes).

    To observe the negative-predictive-value and positive-predictive-value of ThinkSono Guidance triage performance.

Other outcomes

  1. Serial Ultrasound Sensitivity

    Time frame: Measured at the time of ThinkSono Guidance scanning, during scan review by qualified clinicians, and during simulation of serial ultrasound scanning.

    Clinical practice guidelines for proximal compression ultrasound recommend a repeat scan within a week if the initial scan is negative, in order to identify any progression of initially undetectable thrombi. Repeat scans were unfeasible and not clinically indicated for subjects in this study, and this outcome measure was simulated. Further details are available in the trial protocol and statistical analysis plan.

    This figure represents the estimated sensitivity of a repeated ThinkSono Guidance scan for lower extremity proximal DVT 1 week after the initial scan, as per clinical guidelines.

Sponsors and collaborators

Lead sponsor

ThinkSono, Ltd.

Industry

Collaborators

  • Allegheny Health Network
  • NYU Langone Health
  • South Texas Veterans Health Care System
  • Temple Health
  • University of Wisconsin, Madison

Registry information

Acronym: DVT GUARD

Important dates

Study start
2023
Primary completion
2025
Study completion
2025
First posted
Oct 22, 2024
Registry last updated
Jul 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.

Published trials that share one or more normalized conditions with this study.