Skip to content

Fracture Ultrasound in Kids Wirst Trial (FRUSKI-Wrist)

Fracture Ultrasound in Kids Wirst Trial (FRUSKI-Wrist)

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07046793
Acronym
FRUSKI-Wrist
Enrollment
815
Registered
2025-07-02
Start date
2022-05-01
Completion date
2025-04-10
Last updated
2025-07-24

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Fractures in Children

Brief summary

This is a multicenter combined diagnostic accuracy study and observational prospective cohort. Part one aims to confirm non-inferiority of POCUS for the detection of distal forearm fractures compared to X-ray. Part two aims to confirm non-inforiority of POCUS compared to x-ray for the detection of potentially unstable forearm fractures needing follow up imaging.

Interventions

DIAGNOSTIC_TESTPOCUS

Ultrasound screening of the distal forearm.

Sponsors

Luzerner Kantonsspital
CollaboratorOTHER
Insel Gruppe AG, University Hospital Bern
CollaboratorOTHER
University Hospital, Geneva
CollaboratorOTHER
La Tour Hospital
CollaboratorOTHER
Hôpital Fribourgeois
CollaboratorOTHER
University Children's Hospital Basel
CollaboratorOTHER
David Troxler
Lead SponsorOTHER

Study design

Observational model
OTHER
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
No minimum to 18 Years
Healthy volunteers
No

Inclusion criteria

* Patients presenting to the emergency room of a study hospital with an acute trauma to the wrist and suspected fracture of the wrist consulted by a trained study examiner. * Age 0-18 years Depending on the result

Exclusion criteria

* Patient needing immediate medical attention (triage score 1 or 2) as well as severely displaced or open fractures or neurovascular compromise distally to the suspected fracture. * Patient with imaging studies obtained prior to the emergency room visit * Patient with prior fracture of the affected wrist within the last 24 months * Patient refusing participation / missing informed consent.

Design outcomes

Primary

MeasureTime frame
Fracture yes/no as final diagnosisat 4 weeks from inclusion
Possible unstable fracture as final diagnosis4 weeks from inclusion

Countries

Switzerland

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026