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Clinical Trial Details — Status: Recruiting

Administrative data

NCT number NCT04993495
Other study ID # 49RC21_0140
Secondary ID
Status Recruiting
Phase
First received
Last updated
Start date July 7, 2022
Est. completion date July 7, 2023

Study information

Verified date July 2022
Source University Hospital, Angers
Contact Delphine DOUILLET
Phone 0241356650
Email delphine.douillet@chu-angers.fr
Is FDA regulated No
Health authority
Study type Observational

Clinical Trial Summary

Head injuries are a common reason for consultation in emergency departments. The clinical severity of head injury is assessed using the Glasgow Coma Scale (GCS). Between 71% and 97.5% of patients with head trauma seen in the emergency department are considered minor, that is to say with an initial GCS 13 and the consequences are quite variable. Three to 10% of patients will have short, medium or long-term health consequences. According to the studies, there are between 2.1 and 8% of intracranial bleeding immediate or delayed (up to one month), with about 1% of them, the need to resort to neurosurgery. Following a minor head trauma, it is recommended, in the absence of clinical signs of severity, to realize a brain scan (cerebral computerized tomography scan (CT scan): reference imaging examination) within 6h (between 4 hours and 8 hours according to studies), a hospital surveillance of 24h, with the realization of a control scanner within 12 hours to 24 hours in case of treatment by anticoagulants or antiaggregation. In December 2015, Journal of the American Medical Association published an article evaluating two clinical algorithms across the Atlantic, the New Orleans Criteria (NOC) and the Canadian CT Head Rule, to identify a group of patients with a very low risk of severe brain damage. The performance of this score is unquestionably, however, it does not include patients treated with antiplatelet or anticoagulant drugs; risk factors having a decisive impact on the incidence of intracranial bleeding. In this context, various studies have been carried out retrospectively in Angers to assess the incidence and risk factors of the occurrence of an immediate or delayed intracerebral hemorrhage in patients with minor head trauma with or without anti-thrombotic treatment.


Recruitment information / eligibility

Status Recruiting
Enrollment 470
Est. completion date July 7, 2023
Est. primary completion date July 7, 2023
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - patient > 18 years old - head injury - Glasgow Coma Scale > or = 13 Exclusion Criteria: - Refusal of participation, - Indication of a scanner for a reason other than minor head injury - follow-up not possible - pregnant woman or breastfeeding - patients in life-threatening emergency situations.

Study Design


Locations

Country Name City State
France DOUILLET Delphine Angers

Sponsors (1)

Lead Sponsor Collaborator
University Hospital, Angers

Country where clinical trial is conducted

France, 

Outcome

Type Measure Description Time frame Safety issue
Primary intracranial hemorrhage rate in patients in patients considered to be low risk according to the score created by hospital of Angers (negative predictive value). to assess stratification score performance to predict the occurrence of acute intracranial bleeding in patients with minor head injury Day 30
Secondary loss of one point on the rankin scale Performance assessment of hemorrhagic risk stratification score to predict severe intracerebral hemorrhage Day 30
Secondary number of cerebral computerized tomography scan Assessment of the potential reduction in the number of scanners if the score had been applied. Day 30
Secondary time spent in emergencies Retrospective assessment of the potential impact of applying the score on the length of time spent in emergencies Day 1
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