Automated Dating Scan Probe Pressure Data Collection Plan
Sponsor
IntelligentUltrasound Limited (Industry)
Overall Status
Not yet recruiting
CT.gov ID
NCT05963243
Collaborator
(none)
25
4
Study Details
Study Description
Brief Summary
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.
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
|
Study Design
Study Type:
Observational
Anticipated Enrollment
:
25 participants
Observational Model:
Case-Only
Time Perspective:
Prospective
Official Title:
A Volunteer Study to Collect Imaging Data for the Development of Identifying Probe Pressure as Part of ScanNav Assist Automated Dating Scan
Anticipated Study Start Date
:
Aug 1, 2023
Anticipated Primary Completion Date
:
Dec 1, 2023
Anticipated Study Completion Date
:
Dec 1, 2023
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Healthy Volunteers Healthy adult (18+ years old) volunteers |
Other: Ultrasound Scans
Ultrasound scans collected by experts in ultrasound-guided regional anaesthesia.
|
Outcome Measures
Primary Outcome Measures
- Ultrasound scan recordings [6 months]
Ultrasound scan recordings collected by the volunteer healthy participants of an abdominal self-scan.
Eligibility Criteria
Criteria
Ages Eligible for Study:
18 Years
and Older
Sexes Eligible for Study:
All
Accepts Healthy Volunteers:
Yes
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.
Contacts and Locations
Locations
No locations specified.Sponsors and Collaborators
- IntelligentUltrasound Limited
Investigators
- Principal Investigator: Steve Margetts, Dr, Intelligent Ultrasound
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.Responsible Party:
IntelligentUltrasound Limited
ClinicalTrials.gov Identifier:
NCT05963243
Other Study ID Numbers:
- IU2023_WH_02
First Posted:
Jul 27, 2023
Last Update Posted:
Jul 27, 2023
Last Verified:
Jul 1, 2023
Individual Participant Data (IPD) Sharing Statement:
No
Plan to Share IPD:
No
Studies a U.S. FDA-regulated Drug Product:
No
Studies a U.S. FDA-regulated Device Product:
No