NCT06920277

Brief Summary

This study is designed to collect ultrasound images from healthy volunteers in the U.S.

Trial Health

87
On Track

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Enrollment
46

participants targeted

Target at P25-P50 for all trials

Timeline
Completed

Started Oct 2024

Geographic Reach
1 country

1 active site

Status
completed

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

Click on a node to explore related trials.

Study Timeline

Key milestones and dates

Study Start

First participant enrolled

October 29, 2024

Completed
2 days until next milestone

Primary Completion

Last participant's last visit for primary outcome

October 31, 2024

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

October 31, 2024

Completed
5 months until next milestone

First Submitted

Initial submission to the registry

March 25, 2025

Completed
15 days until next milestone

First Posted

Study publicly available on registry

April 9, 2025

Completed
Last Updated

April 9, 2025

Status Verified

April 1, 2025

Enrollment Period

2 days

First QC Date

March 25, 2025

Last Update Submit

April 2, 2025

Conditions

Ultrasound Scan

Keywords

Data collectionArtificial IntelligenceRegional Anesthesia

Outcome Measures

Primary Outcomes (1)

  • Number of ultrasound scan recordings relevant to peripheral nerve blocks collected

    Ultrasound scans will be collected and reviewed for quality and completeness. The outcome will be the number of ultrasound recordings that meet predefined criteria for image quality; correct anatomical region and clear visualization to support AI development.

    Day 1, 2 and 3

Study Arms (1)

U.S. population

Device: Ultrasound scans

Interventions

Ultrasound scansDEVICE

10 seconds scanning for one block region

U.S. population

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersYes
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

volunteers from the U.S. population

You may qualify if:

  • Provision of signed and dated informed consent form
  • At least 18 years of age and older
  • Stated willingness to comply with all study procedures and availability for the duration of the study
  • In good general health

You may not qualify if:

  • Pregnancy
  • Inability to lie to flat
  • Any complaint or anatomical deformity on the regions to be scanned

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Conference Room at Doubletree by Hilton Austin

Austin, Texas, 78752, United States

Location

Study Officials

  • Senanur Samur Duysal

    Smart Alfa Teknoloji San. ve Tic. A.S.

    PRINCIPAL INVESTIGATOR

Study Design

Study Type
observational
Observational Model
CASE ONLY
Time Perspective
PROSPECTIVE
Sponsor Type
INDUSTRY
Responsible Party
SPONSOR

Study Record Dates

First Submitted

March 25, 2025

First Posted

April 9, 2025

Study Start

October 29, 2024

Primary Completion

October 31, 2024

Study Completion

October 31, 2024

Last Updated

April 9, 2025

Record last verified: 2025-04

Data Sharing

IPD Sharing
Will not share

Locations

US(1)