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Clinical Trials/NCT02828527
NCT02828527
Completed
Not Applicable

Care Courses for Mild Head Injury Patients

Fondation Hôpital Saint-Joseph1 site in 1 country50 target enrollmentSeptember 12, 2014

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Mild Head Injury
Sponsor
Fondation Hôpital Saint-Joseph
Enrollment
50
Locations
1
Primary Endpoint
Assessment of change in Glasgow score
Status
Completed
Last Updated
8 years ago

Overview

Brief Summary

Background / Rationale at. The mild head injury.

In France, the incidence of head injuries is estimated at 100,000 per year in France. 80% of mild head trauma. This is a pattern of frequent use of the health system. The reason for consultation, benign appearance, present a significant risk of complication. In 15 to 25% of the evolution of head injury is unfavorable. Disorders of attention, memory disorders, psychiatric events and mood changes may occur. These symptoms are grouped into a syndrome, post-concussion syndrome.

The post-concussion syndrome:

It affects approximately 20,000 people per year in France. This is a common disease and most undervalued in the general population. diagnostic criteria post-concussional disorder according to DSM-IV (Diagnostic and Statistical Manual). Symptoms may persist for more than 3 months after head injury. This syndrome is responsible for suffering, personal and professional sound and quality of life of patients. It is particularly debilitating in everyday life, and can have disastrous consequences on their family, social, cultural and professional. It gives rise to many financial implications with compensation requirements and expertise consultations.

Intention of work In a recent study by a team of neuropsychologists Kremlin Bicetre, it has been shown that screening and early treatment of post-concussion syndrome from the slight head injury prevents chronicity of symptoms.

Detailed Description

Methodology : Design: Cohort study single-center prospective observational. Recruitment period: 15/11/2014 to 15/12/2014 approximately (50 records necessary). Then follow a month is required. Either theoretical study end: 01/15/2015. Acquisition of data: Pre inclusion of patients in the study by sorting CAE emergency department on the following host pattern: traumatic brain injury with loss of consciousness, traumatic brain injury without loss of consciousness, with loss of consciousness discomfort, discomfort without a loss of consciousness peripheral vascular accident PVA. Collection address, telephone number and an e-mail address of the patient (after delivery of a newsletter). call the patient and questionnaire submitted between 0 and J15 and J15 and J30 between.

Registry
clinicaltrials.gov
Start Date
September 12, 2014
End Date
January 1, 2018
Last Updated
8 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Sponsor

Eligibility Criteria

Inclusion Criteria

  • Traumatic brain injury
  • Head injury with loss of consciousness
  • Cranio facial trauma
  • Peripheral vascular accident
  • Discomfort
  • Discomfort with loss of consciousness
  • Before Inclusion Criteria:
  • Head trauma notion AND at least one of the following criteria:
  • Loss of consciousness \<30 minutes
  • Glasgow between 13 and 15

Exclusion Criteria

  • Major Trust
  • Context of acute alcohol (\> 3 glasses) or toxic taking (drugs)
  • Not understanding or communication
  • Patient Refusal

Outcomes

Primary Outcomes

Assessment of change in Glasgow score

Time Frame: submitted between Day 0 and Day 15 and between Day 15 and Day 30

Study Sites (1)

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