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Post Traumatic Critical Complications: a Prospective Cohort Study (ATLANREA)

N

Nantes University Hospital (NUH)

Status

Enrolling

Conditions

Severe Trauma (With or Without Traumatic Brain Injury)

Treatments

Other: Collection of medical data from ICU patients

Study type

Observational

Funder types

Other

Identifiers

NCT02426255
RC12_0207 cohorte fiche 2

Details and patient eligibility

About

The purpose of this observational epidemiological study is to investigate the management and the complications associated with severe trauma. Data will be analysed to answer pre-defined scientific projects and to improve management of these conditions.

Full description

Pseudonymized data will be collected by study coordinators in a secured e-database.

Cross audit will be performed to check data.

Enrollment

5,000 estimated patients

Sex

All

Ages

15+ years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • severe trauma
  • and/or traumatic brain injury
  • and/or hemorrhage

Exclusion criteria

  • Consent withdrawal

Trial design

5,000 participants in 1 patient group

ICU patients
Description:
Patients with severe trauma (with or without brain injury) or Patients with hemorrhagic shock Data concerning the ICU stay will be collected for these patients
Treatment:
Other: Collection of medical data from ICU patients

Trial contacts and locations

5

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Central trial contact

Antoine Roquilly, MD; Karim Asehnoune, PhD, MD

Data sourced from clinicaltrials.gov

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