Actively Recruiting
Prognostic Value of Capillary Lactatemia in Potentially Severe Polytrauma Patients
Led by Centre Hospitalier Universitaire de Nice · Updated on 2026-03-30
550
Participants Needed
3
Research Sites
96 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Nowadays, the tools available to assess the severity of a polytrauma patient in the pre-hospital setting (vital parameters, shock index, MGAP score, Vittel criteria) have their limitations and are sometimes subjective. To date, there are no objective, practical and reproducible tools for triaging these patients. Venous lactataemia also appears to be predictive of poor outcome in severe trauma. However, there are no studies in the literature on capillary lactataemia, which would indicate the potential severity of a polytrauma patient in the pre-hospital setting. However, it is an easily performed, risk-free assay, the results of which can be obtained rapidly at the scene of the accident. The aim of this project is to confirm that, like venous lactataemia, capillary lactataemia can be useful in the pre-hospital phase for predicting a patient's poor outcome. Incorporating this assay into the assessment of potentially severe polytrauma patients in the pre-hospital phase could improve the predictive value of clinical and contextual data and thus enable better referral and management of these patients.
CONDITIONS
Official Title
Prognostic Value of Capillary Lactatemia in Potentially Severe Polytrauma Patients
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patient over 18 years of age
- Presenting a potentially serious pre-hospital trauma defined by a road accident or a fall of more than 2 metres
- Requiring the dispatch of a SMUR 06 mobile emergency and resuscitation team
- Transferred to an emergency facility in the Alpes Maritimes with medical assistance
- Consent signed by the patient or a relative after the event if immediate signing is not possible
- Pregnant women may participate without risk to themselves or their child
You will not qualify if you...
- Patients with isolated peripheral limb trauma (wrist, elbow, knee, ankle, shoulder)
- Patients under legal protection (guardianship, curatorship)
- Patients in cardiorespiratory arrest when taken into care by the SMUR emergency medical services
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Trial Site Locations
Total: 3 locations
1
Antibes Hospital
Antibes, France, 06400
Not Yet Recruiting
2
Cannes hospital
Cannes, France, 06000
Not Yet Recruiting
3
Nice University Hospital
Nice, France, 06000
Actively Recruiting
Research Team
M
Marta FERNANDES FEIRRERA, PH
CONTACT
How is the study designed?
Study Type
INTERVENTIONAL
Masking
NONE
Allocation
NA
Model
SINGLE_GROUP
Primary Purpose
OTHER
Number of Arms
1
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