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Clinical Trials/NCT03810222
NCT03810222
Completed
Not Applicable

A Prospective Outcome Study in Patients With Moderate to Severe Traumatic Brain Injury in Bergamo Area (Italy)

FROM- Fondazione per la Ricerca Ospedale di Bergamo- ETS1 site in 1 country225 target enrollmentJanuary 18, 2017

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Brain Injuries, Traumatic
Sponsor
FROM- Fondazione per la Ricerca Ospedale di Bergamo- ETS
Enrollment
225
Locations
1
Primary Endpoint
Glasgow Outcome Scale - Extended (GOSE)
Status
Completed
Last Updated
5 years ago

Overview

Brief Summary

Traumatic brain injury (TBI) is the leading cause of death, disability and cognitive impairment in young people worldwide. The majority of the traumatic deaths in developed countries results directly from lesions in the central nervous system. Furthermore, due to the persistence of disabling effects of TBI for many years, personal and public costs of supporting survivors have to be taken in consideration.

Many patients rescued by ICU treatment may have been severely disabled or vegetative because of trauma. These data suggest that, despite improvement in medical and surgical treatments, other factors related to trauma itself and to patient's condition could have an impact on the final outcome.

Aim of the TBI-PRO project is to collect high quality clinical and epidemiological data and to describe the outcome of moderate-to-severe TBI in a local contest (Bergamo area, Italy).

Detailed Description

All patients admitted to the ICU with a diagnosis of moderate-to-severe TBI, with or without polytrauma, are recruited. Bergamo hospital is the main Trauma Centre (Level I) and the only referring neurosurgical center within a population of 1.2 million inhabitants of Bergamo area. This hospital is also a Regional Pediatric Trauma Centre.

Registry
clinicaltrials.gov
Start Date
January 18, 2017
End Date
January 31, 2020
Last Updated
5 years ago
Study Type
Observational
Sex
All

Investigators

Sponsor
FROM- Fondazione per la Ricerca Ospedale di Bergamo- ETS
Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • admission to ICU
  • diagnosis of moderate-to-severe TBI

Exclusion Criteria

  • Patients who died in the first couple of hours after hospital admission are not included.

Outcomes

Primary Outcomes

Glasgow Outcome Scale - Extended (GOSE)

Time Frame: 12 Months Post-Injury

The global functional outcome at 12 months is assessed using the Glasgow Outcome Scale-Extended (GOS-E), obtained through structured interview. The GOS-E is a well-validated, widely employed measure of disability based on information on independence, employability, and social/community participation. The baseline function prior to injury is assessed to ensure that the deficit can be attributed to the event. GOS-E is dichotomized into favorable (a score of 5 to 8, Moderate Disability is defined by a score of 5-6) and unfavorable (a score of 1 to 4, Dead is defined by a score of 1).

Secondary Outcomes

  • Neuropsychological evaluation(12 Months Post-Injury)
  • 6-Month Outcome(6 Months Post-Injury)

Study Sites (1)

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