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Completed

NCT Number: NCT03293420

Retrospective Analysis of a Population of Patients With With Severe Traumatic Head Injury and Woken Early

Observational retrospective study that included all patients meeting the inclusion criteria from 1st January 2014 to 31st December 2015.

The objective of the study is to describe and compare two populations of patients with severe traumatic head injury arriving under sedation in the Department in whom the sedation was not continued.

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Key information

Conditions

Traumatic Head Injury

Age range

18 year and older

Sex eligibility

All sexes

Study type

Observational

Primary location

CHU Dijon Bourgogne

Dijon, France

Who can participate

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with traumatic head injuring arriving in the Neurosurgery and Traumatologic Intensive Care Unit under sedation

Exclusion criteria

  • Brain death within the 48h following admission,
  • Stroke leading to the traumatic head injury,
  • Death within the 24h following admission,
  • Patients not under sedation on admission to the unit,
  • Non-sedated patients transferred directly to the operating theatre
  • Traumatic brain injury in patients presenting chronic sub-dural haematoma,
  • Continued sedation (> 15h) in the ICU.

Treatment and study plan

Primary outcomes

  1. Motor score

    Time frame: At baseline

Sponsors and collaborators

Lead sponsor

Centre Hospitalier Universitaire Dijon

Other

Registry information

Acronym: PRECOCE TC

Important dates

Study start
2016
Primary completion
2016
Study completion
2016
First posted
Sep 26, 2017
Registry last updated
Sep 26, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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