IPSTRAUC : Impact on Care Pathways of a New Management of Cervical Trauma in Conscious Patients Stable in Pre-hospital Care

Recruiting N/A Interventional Study
Prehospital Emergency Neck Injury Neck Trauma Emergency Medical Services
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 – 65
Sex
Any
Study type
Interventional
Purpose
Diagnostic
Participants needed
840 (estimated)
Sponsor
Rennes University Hospital · Other
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About This Trial

The aim of the study is to evaluate the application of Canadian C-Spine rules adapted to pre-hospital settings in France in order to improve the appropriateness of cervical spine immobilisation, reduce unnecessary imaging examinations and optimise patient care pathways.

Trial Locations
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Eligibility Criteria
Inclusion Criteria: PATIENTS * GCS 15 * Stable (no organ failure, SBP ≥ 90 mmHg, DBP ≥ 65 mmHg, RF between 10 and 24 cycles/min) * Cooperative (calm and obedient to instructions) * Victim of a closed cervical spine trauma treated in the pre-hospital setting (fire brigade and/or Mobile Emergency an…
Contacts

Marie-Laure Gervais, PhD

2 99 28 25 91

marie-laure.gervais@chu-rennes.fr

CONTACT