NCT06551350 Retrospective Assessment of Referral of a Major Trauma Patient
| NCT ID | NCT06551350 |
| Status | Recruiting |
| Phase | — |
| Sponsor | Hôpital NOVO |
| Condition | Trauma Injury |
| Study Type | OBSERVATIONAL |
| Enrollment | 461 participants |
| Start Date | 2024-10-18 |
| Primary Completion | 2025-05 |
Eligibility & Interventions
Eligibility Fast-Check
Enter your details for a quick preliminary check. This does not replace medical advice.
What to Expect as a Participant
This is an observational study. You will not receive an experimental treatment; researchers will collect data based on your existing condition or standard treatment.
This trial targets 461 participants in total. It began in 2024-10-18 with a primary completion date of 2025-05.
⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.
Brief Summary
The aim of this study is to find out whether major trauma patients from the Val d'Oise are referred to the appropriate trauma centre for their care and to assess the quality of triage within the Val d'Oise department.
Eligibility Criteria
Inclusion Criteria : * Between the 1st January 2023 and the 31th December 2023 * Regulated by SAMU 95 with suspected major trauma * Sending an MCIU * At least 1 Vittel criterion\* Exclusion Criteria : * Death on site * Care by an MICU team outside the 95 * Minor patients and legal protection * Transport refusals * Vittel criterion : • Physiological variables : Glasgow score \< 13 Systolic blood pressure \< 90 mmHg O2 saturation \< 90% • Elements of kinetics : Ejection from a vehicle Other passenger killed in the same vehicle Fall \> 6 metres Victim thrown or crushed Overall assessment (deformation of the vehicle, estimated speed, absence of helmet, absence of seatbelt) Blast • Anatomical lesions : Penetrating trauma to the head, neck, thorax, abdomen, pelvis, arm or thigh Flail chest Severe burn, smoke inhalation Pelvic fracture Suspected spinal cord injury Amputation of wrist, ankle or above Acute limb ischaemia • Pre-hospital resuscitation : Assisted ventilation Filling \> 1000 ml with colloids Catecholamines Inflated shock-proof trousers • Medical context (to be assessed) : Age \> 65 Cardiac or coronary insufficiency Respiratory insufficiency Pregnancy (2nd and 3rd trimesters) Blood crase disorders
Contact & Investigator
Fabrice LOUVET
PRINCIPAL INVESTIGATOR
Hôpital NOVO
Frequently Asked Questions
Who can join the NCT06551350 clinical trial?
This trial is open to participants of all sexes, aged 18 Years or older, studying Trauma Injury. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.
Is NCT06551350 currently recruiting?
Yes, NCT06551350 is actively recruiting participants. Contact the research team at maryline.delattre@ght-novo.fr for enrollment information.
Where is the NCT06551350 trial being conducted?
This trial is being conducted at Pontoise, France.
Who is sponsoring the NCT06551350 clinical trial?
NCT06551350 is sponsored by Hôpital NOVO. The principal investigator is Fabrice LOUVET at Hôpital NOVO. The trial plans to enroll 461 participants.