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Pre-hospital Notification of Injured Patients Presenting to Trauma Centres in India

Reducing the Burden of Injury in India and Australia Through Development and Piloting of Improved Systems of Care - Prehospital Notification and Structured Handover on Hospital Arrival

Status
UNKNOWN
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT02877342
Enrollment
500
Registered
2016-08-24
Start date
2016-03-31
Completion date
2018-02-28
Last updated
2016-08-24

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

Conditions

Major Trauma

Keywords

Injury, Injuries, Triage

Brief summary

A prospective observational study using an interrupted time-series design to evaluate the effect of pre-hospital notification on trauma patients arriving at a trauma centre by ambulance, in India

Detailed description

This is a longitudinal prospective cohort study of injured patients being transported by ambulance to the major trauma centre study sites. In the pre-intervention phase, prospective data on patients will be collected on pre-hospital assessment, notification, in-hospital assessment, management and outcomes and recorded in a new tailored multi-hospital trauma registry. All injured patients arriving by ambulance and allocated to a red or yellow priority category will be eligible for inclusion. The intervention will be a pre-hospital notification application in the form of an Android program that will be used by ambulance clinicians to notify emergency departments of selected hospitals of an impending arrival of a patient. The application will use a simple algorithm based on trauma triage principles developed by the Australia-India Trauma System Collaboration (AITSC). The proportion of severely injured patients arriving to hospital after notification will be the primary outcome measure with a target of 70%. Secondary outcomes evaluated will be availability of a trauma cubicle, presence of a trauma team on patient arrival, time to first chest x-ray and in-hospital mortality.

Interventions

OTHERPre-hospital notification

Pre-hospital notification smartphone/tablet application in the form of an Android program that will be used by ambulance clinicians to notify emergency departments of selected hospitals of an impending arrival of a patient.

Sponsors

National Trauma Research Institute
CollaboratorOTHER
The Alfred
CollaboratorOTHER
Monash University
CollaboratorOTHER
All India Institute of Medical Sciences
CollaboratorOTHER
The George Institute for Global Health, Australia
CollaboratorOTHER
Sheth Vadilal Sarabhai General Hospital
CollaboratorOTHER
Guru Teg Bahadur Hospital
CollaboratorOTHER
Lokmanya Tilak Municipal Medical College and Hospital
CollaboratorOTHER
Centralised Accident and Trauma Services, Delhi, India
CollaboratorOTHER_GOV
GVK EMRI: Emergency Management and Research Institute
CollaboratorOTHER
Maharashtra Emergency Medical Services, India
CollaboratorOTHER
Nathiba Hargovandas Lakhmichand Municipal Medical College, India
CollaboratorUNKNOWN
University College of Medical Sciences, India
CollaboratorINDIV
Teresa Howard
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

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

Inclusion criteria

All injured patients arriving by ambulance and allocated to a red (1st) or yellow (2nd) priority category will be eligible for inclusion. Data will be collected prospectively by trained data collectors positioned in the trauma centres. Retrospective inclusion will be continued for all screened patients presenting to any of the included hospitals with injury (including near-drowning) as the primary diagnosis and with at least one of the following criteria: 1. Admission to hospital 2. Death after triage but before admission 3. Dead on arrival

Exclusion criteria

Patients meeting screening criteria will be subsequently excluded if they meet any of the following criteria: 1. Dead at scene 2. Alive at triage but not admitted to hospital (discharged alive) 3. Isolated poisoning 4. Isolated burns 5. Single digit finger or toe amputations (unless of the thumb or great toe), only

Design outcomes

Primary

MeasureTime frameDescription
Pre-hospital notification1 - 1.5 yearsPrior to arrival at emergency department. Pre-hospital notification will be the primary outcome, defined as a phone call or message to a treating hospital clinician regarding an injured patient enroute to hospital. For the purpose of this research project, a patient will satisfy primary outcome criteria if pre-hospital notification with any information has occurred. This variable will be collected and analysed as a binary variable.

Secondary

MeasureTime frameDescription
Presence of trauma team leader1 - 1.5 yearsTrauma leader is present when the patient enters the emergency department for treatment. The presence of a trauma team leader at the time of patient arrival will be collected as a binary variable. This is the person whose role is to co-ordinate the trauma resuscitation
Readiness of trauma bay1 - 1.5 yearsAt least 1 trauma bay that has been allocated and empty (therefore ready to receive a patient) on arrival.
Trauma Call out1 - 1.5 yearsA trauma callout occurs in response to the notification. A trauma call-out will be recorded as a binary variable- whether one has occurred or not.
Location of patient discharge1 - 1.5 yearsThe location to which a patient was discharged on completion of hospital management will be recorded
In-hospital death1 - 1.5 yearsPatient death whilst in hospital
Time to first chest x-ray1 - 1.5 yearsTime at which the first chest x-ray commenced will be recorded.

Countries

India

Contacts

Primary ContactMathew Joseph, MBBS
joseph.mathew@monash.edu+613431618029
Backup ContactBiswadev Mitra, MBBS, PhD
biswadev.mitra@monash.edu+613402095415

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 26, 2026