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Fast Track for Wrist and Scaphoid Fractures

Fast Track in the Emergency Department for Wrist and Scaphoid Fractures: a Randomised Trial

Status
Terminated
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT05183477
Enrollment
196
Registered
2022-01-10
Start date
2021-12-17
Completion date
2024-09-30
Last updated
2025-02-27

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

Conditions

Scaphoid Fracture, Wrist Fracture

Brief summary

This is a mono centric, prospective, randomised trial on the implementation and assessment of a shortened pathway for mono-trauma of the wrist and suspected fracture of distal radius and/or ulna and/or scaphoid bone.

Detailed description

Patients will be randomised into two groups: fast track and normal pathway. At the arrival in the Emergency Department a triage will be performed. In case of met inclusion criteria the patient will sign the informed consent and will be randomised in one of the two study groups. The fast track group will be straightforwardly evaluated for absence of exclusion criteria (in case of exclusion criteria present the investigators will follow the normal pathway and the patient will not be included in the study). Then, patients will be assessed with an ad hoc checklist and then sent for x-ray performance, if necessary. After the x-ray the patients will be examined by an emergency physician that will have the opportunity to request new x-ray views if necessary. The normal pathway group will go straight to medical examination as soon as possible, depending on waiting times in the Emergency Department. Investigators will collect anagraphical data, waiting times, time to x-ray, overall length of stay in the Emergency Department, patients' and staff's satisfaction for the two groups.

Interventions

short cut for the request of xrays directly at triage

OTHERnormal pathway

x-ray would be required according to doctor's clinical evaluation.

Sponsors

Ente Ospedaliero Cantonale, Bellinzona
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

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

Inclusion criteria

* adults patients presenting at the emergency dept with suspected scaphoid or wrist fracture * monotrauma * written informed consent

Exclusion criteria

* patients younger than 18 yr * pregnant women * either vascular or neural impairment * signs of open fracture * multiple trauma patient

Design outcomes

Primary

MeasureTime frameDescription
number of x rays requestedFrom admission to discharge, up to 2.5 hoursthe number of xray requested

Secondary

MeasureTime frameDescription
patient's satisfactionFrom admission to discharge, up to 2.5 hoursPatients' satisfaction will be tested with the help of the brief emergency department patient satisfaction scale (BEPSS). The questionnaire consists of 20 questions and for each item, a response scale form 1 (completely disagree) to 4 (completely agree) is used.
waiting time before examinationFrom admission to discharge, up to 2.5 hours
waiting time before xrayFrom admission to discharge, up to 2.5 hours
total length of stay in the emergency departmentFrom admission to discharge, up to 2.5 hours

Countries

Switzerland

Outcome results

None listed

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