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PariS-TBI Study : Paris Severe Traumatic Brain Injury Study

NCT01437683 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 252

Last updated 2012-10-15

No results posted yet for this study

Summary

The primary objective of the protocol is to study the long-term outcome of a large group of traumatic brain injury patients.

This outcome is to be described in terms of activity, participation, quality of life, SOCIO-professional outcome and impact on caregivers, and in relation to health care provision.

The secondary outcome is to measure the impact on functional outcome of several predictive factors, and their relative importance on outcome. Our principal hypothesis is that SOCIO-professional and health provision factors play a major role on long-term outcome, further even than initial severity of brain injury.

Conditions

  • Brain Injury
  • Craniocerebral Trauma
  • Trauma Nervous System

Sponsors & Collaborators

  • Institut de Recherche en Santé Publique, France

    collaborator OTHER

  • CRFTC

    collaborator UNKNOWN

  • Caisse Nationale de Solidarité pour l'Autonomie

    collaborator OTHER

  • Institut National de la Santé Et de la Recherche Médicale, France

    collaborator OTHER_GOV

  • HAS

    collaborator UNKNOWN

  • DREES

    collaborator UNKNOWN

  • Assistance Publique - Hôpitaux de Paris

    lead OTHER

Principal Investigators

  • Philippe AZOUVI, PU-PH · APHP

Eligibility

Min Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-02-28
Primary Completion
2011-10-31
Completion
2012-06-30

Countries

  • France

Study Locations

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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 NCT01437683 on ClinicalTrials.gov