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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05765045
Other study ID # TRINU-RX
Secondary ID
Status Completed
Phase N/A
First received
Last updated
Start date March 6, 2023
Est. completion date April 23, 2023

Study information

Verified date June 2023
Source Universiteit Antwerpen
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In 2019, nearly half of all hospital contacts in Belgium took place through the emergency department, and more than a third of patients arrived after an accident or trauma. In instances of overcrowding, patients with minor orthopedic injuries face prolonged waiting times. Previous studies have shown that implementing triage protocols for medical imaging conducted by a triage nurse can reduce the Total Length of Stay (TLOS) for this patient group. This is a single-center, unblinded, randomized, controlled trial that aims to evaluate the impact of a nurse triage protocol on turnaround time (primary outcome), quality of care, and patient satisfaction. The study population consists of adults who present with minor orthopedic injuries below the elbow or knee and have an Emergency Severity Index (ESI) of 4 or 5. Participants are randomly assigned to either the 'nurse triage protocol' group (n=110) or the 'usual care' group (n=110).


Recruitment information / eligibility

Status Completed
Enrollment 220
Est. completion date April 23, 2023
Est. primary completion date April 23, 2023
Accepts healthy volunteers Accepts Healthy Volunteers
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Adults (18 years old) - ESI 4 or ESI 5 Recent trauma (< 10 days after trauma) - Accidental trauma mechanism - Trauma below the elbow (forearm, wrist, hand, finger) - Trauma below the knee (lower leg, ankle, foot, toe) Exclusion Criteria: - ESI 1 or ESI 2 or ESI 3 - Return visit after previous emergency department contact for the same injury (e.g. increased pain, tight cast, ...) - Trauma resulting from underlying somatic pathology (e.g. syncope, epileptic attack, vertigo, vasovagal collapse, ...) - Atraumatic (pain) complaints (e.g. pain in the calf, toe, foot, wrist, ... without a clear trauma mechanism) - Additional, non-orthopedic injuries (e.g. laceration, signs of cerebral commotion, ...) - Pregnancy or a suspicion of pregnancy

Study Design


Related Conditions & MeSH terms


Intervention

Diagnostic Test:
Nursing triage protocol
Medically approved and supervised standing order that allows trained ER nurses to start medical imaging (RX) for adult patients with minor traumata to the limbs.

Locations

Country Name City State
Belgium University of Antwerp Wilrijk Antwerp

Sponsors (2)

Lead Sponsor Collaborator
Universiteit Antwerpen Heilig Hartziekenhuis, Mol

Country where clinical trial is conducted

Belgium, 

Outcome

Type Measure Description Time frame Safety issue
Primary TLOS Total length of stay 6-8 weeks
Secondary Patient satisfaction Patient satisfaction measured by a 10-point Likert scale at discharge using a questionnaire 6-8 weeks
Secondary Treatment efficiency Measurement if the patient diagnosis and/or treatment was correctly initiated at the Emergency Department. Yes = no additional diagnosis or treatments were necessary; No = within 14 days after discharge a change in treatment or new diagnosis was done. Data will be collected using the hospital's patient records or by calling patients if no information is found in the record. 6-8 weeks
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