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

NCT02877342 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 500

Last updated 2016-08-24

No results posted yet for this study

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

Conditions

  • Major Trauma

Interventions

OTHER

Pre-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 & Collaborators

  • National Trauma Research Institute

    collaborator OTHER
  • The Alfred

    collaborator OTHER
  • Monash University

    collaborator OTHER
  • All India Institute of Medical Sciences

    collaborator OTHER
  • The George Institute for Global Health, Australia

    collaborator OTHER
  • Sheth Vadilal Sarabhai General Hospital

    collaborator OTHER
  • Guru Teg Bahadur Hospital

    collaborator OTHER
  • Lokmanya Tilak Municipal Medical College and Hospital

    collaborator OTHER
  • Centralised Accident and Trauma Services, Delhi, India

    collaborator OTHER_GOV
  • GVK EMRI: Emergency Management and Research Institute

    collaborator OTHER
  • Maharashtra Emergency Medical Services, India

    collaborator OTHER
  • Nathiba Hargovandas Lakhmichand Municipal Medical College, India

    collaborator UNKNOWN
  • University College of Medical Sciences, India

    collaborator INDIV
  • Teresa Howard

    lead OTHER

Principal Investigators

  • Mark C Fitzgerald, MBBS, MD · National Trauma Research Institute

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2016-03-31
Primary Completion
2017-08-31
Completion
2018-02-28

Countries

  • India

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02877342 on ClinicalTrials.gov