Automated Dating Scan Probe Pressure Data Collection Plan

The goal of this observational study is to collect data in the form of ultrasound recordings from healthy volunteers, to aid the development of an Artificial Intelligence model that can identify ultrasound probe pressure.

Completed

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Key information

Conditions

Ultrasound

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

Hodge House

Cardiff, CF10 1DY, United Kingdom

Who can participate

Healthy volunteers accepted: Yes

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

Inclusion criteria

Male or female, at least 18 years of age;
Able to comprehend and sign the Informed Consent prior to enrolment in the study.

Exclusion criteria

Aged <18 years of age;
Unwilling or unable to provide informed consent.

Treatment and study plan

Ultrasound scans

Other

Ultrasound scans collected by experts in ultrasound-guided regional anaesthesia.

Primary outcomes

Ultrasound scan recordings

Time frame: 6 months

Ultrasound scan recordings collected by the volunteer healthy participants of an abdominal self-scan.

Interested in participating?

Completed

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Sponsors and collaborators

Lead sponsor

IntelligentUltrasound Limited

Industry

Registry information

Official study title

A Volunteer Study to Collect Imaging Data for the Development of Identifying Probe Pressure as Part of ScanNav Assist Automated Dating Scan

Important dates

Study start: 2023
Primary completion: 2023
Study completion: 2024
First posted: Jul 27, 2023
Registry last updated: Mar 28, 2024

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.

Completed