Structured Trauma Quality Improvement Meetings at Four Trauma Centres in India

NCT03005509 · Status: COMPLETED · Phase: NA · Type: INTERVENTIONAL · Enrollment: 1500

Last updated 2019-11-27

No results posted yet for this study

Summary

A prospective before-and-after study to evaluate the effect of implementing a Trauma Quality Improvement protocol on the process of Trauma Quality Improvement meetings and major trauma patient outcomes at four trauma centres in India.

Conditions

  • Major Trauma
  • Injuries Major

Interventions

OTHER

TQIM checklist

The intervention phase will include an intense training period covering: 1. Conduct of Trauma Quality Improvement Meeting (TQIM) (and Trauma Quality Improvement program in general). The training will be delivered using the World Health Organization (WHO) Trauma Quality Improvement Programmes short course and online resources. 2. Implementation of Trauma Quality Improvement Meeting (TQIM) Checklist.

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
  • Dr Gerard O'Reilly

    lead OTHER

Principal Investigators

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

Study Design

Allocation
NON_RANDOMIZED
Purpose
OTHER
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2017-01-31
Primary Completion
2018-03-31
Completion
2018-03-31

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 NCT03005509 on ClinicalTrials.gov