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Trauma Triage Decision With Software (TraumaDS)

Triage With Software Assistance To Trauma Patient Who Attending To Emergency Department

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03357835
Acronym
TraumaDS
Enrollment
1000
Registered
2017-11-30
Start date
2017-11-01
Completion date
2018-03-30
Last updated
2017-11-30

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

Conditions

Trauma, Triage

Keywords

trauma, triage, software, emergency

Brief summary

It is intended to show that a computer software called Trauma Decision System (TravmaDS) for the determination of the urgency of trauma patients who applied to Emergency Medical Clinic gives more accurate, more objective, faster results than the triage scored by medical and non-medical personnel and to show the fact that TraumaDS provides more patient satisfaction.

Detailed description

There are limitations in our routine standard of practice in Emergency medical clinic in rapid triage about the adequacy particularly in the patient group where specific and rapid decision-making, such as trauma. The process of evaluating the patients who are directed to the green area unnecessarily in trauma care by the physician is prolonged, the evaluation process of patients who are directed to the red area unnecessarily shortens but hospital resources are being used extensively. Therefore, in this study, it was planned to perform objective triage with a computer based scoring system. Triage scoring determined by the Ministry of Health (SB ), routinely performed by an emergency medical technician (EMT), will be applied when the patients are admitted to emergency services. According to this scoring, patients who need urgent care and who should not wait less than 15 minutes will be considered red coded, patients who can wait up to 60 minutes will be considered yellow coded, patients who can wait for 120 minutes or more will be considered green coded. To the other group, triage maintenance / evaluation will be done with computer software developed by us. All patients with trauma should be included in the study, demographic data, trauma mechanism and trauma type vital signs at the time of application of the patients will be routinely observed in both groups of patients. These observations are routine for this disease group and we will not undertake any interventional procedures or screening except special routine application for research purposes. The observation and file information will be organized by the triage staff in both groups at the time of the application of the patients. In this software-based program before working on the software informative training will be given to triage staff and for this patient triage handheld computers will be given to triage staff. In order for the referring patients to be able to see the entries made with the triage software a simultaneous large-screen monitor will be used. At the time of application, color codes indicating the urgency of the patients will be given according to the demographic data of the patients, the type of trauma and the vital signs were directed by the software program. As a result of the software program's direction, patients will be coded as green-yellow-orange-red area and patient care will be made in accordance with these codes.

Interventions

OTHERTrauma Decision System

At the time of application, color codes indicating the urgency of the patients will be given according to the demographic data of the patients, the type of trauma and the vital signs were directed by the software program. As a result of the software program's direction, patients will be coded as green-yellow-orange-red area and patient care will be made in accordance with these codes.

Sponsors

Derince Training and Research Hospital
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Healthy volunteers
No

Inclusion criteria

* all trauma patients who want to participate

Exclusion criteria

* who do not want to participate, who are not triaged, who leave the hospital before the treatment is completed

Design outcomes

Primary

MeasureTime frameDescription
Difference between software triage time and traditional triage time5 minutesInvestigation difference of triages made by software and normal triage

Secondary

MeasureTime frameDescription
30-day mortality30 daysDefined as mortality within 30 days of arrival to hospital

Countries

Turkey (Türkiye)

Contacts

Primary ContactAhmet Akdoğan, RA
ahmetakd@hotmail.com+905056773379
Backup ContactOnur Karakayalı, Specialist
dr_onurkarakayali@hotmail.com+90 0506 3284484

Outcome results

None listed

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