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Impact of a Magnetic Resonance Imaging (MRI) Scanner Exclusively Dedicated to Emergency in the Clinical Management of Patients Presenting With Diplopia or Dizziness

Impact of a Magnetic Resonance Imaging (MRI) Scanner Exclusively Dedicated to Emergency in the Clinical Management of Patients Presenting With Diplopia or Dizziness

Status
Completed
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT03660852
Acronym
IRM-DU
Enrollment
119
Registered
2018-09-07
Start date
2018-07-24
Completion date
2020-01-24
Last updated
2023-07-14

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Diplopia, Dizziness, Emergency Department, MRI, Stroke

Brief summary

IRM-DU is a prospective observational single center study conducted in an emergency department to evaluate the impact of a MRI scanner exclusively dedicated to emergency in the clinical management of patients presenting with dizziness or diplopia. The study will compare 2 strategies : after and before availability of a MRI scanner dedicated to emergency. The primary endpoint is the proportion of patients with a diagnosis of stroke confirmed by imaging (MRI or Computed tomography (CT)) in the group before implementation of the emergency MRI scanner and the group after implementation of the emergency MRI scanner. The hypothesis is that the availability of a MRI scanner dedicated to emergency will improve the diagnosis of stroke in patients presenting with dizziness or diplopia, and will reduce Emergency Department stay, hospital stay and hospitalisation costs.

Interventions

None listed

Sponsors

University Hospital, Strasbourg, France
Lead SponsorOTHER

Study design

Observational model
CASE_CONTROL
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* age over 18 years * non opponent to participate * dizziness or diplopia requiring brain imaging in order to eliminate stroke

Exclusion criteria

* opponent to participate * pregnant women * recent cerebral trauma * potentially eligible to thrombolysis * impaired consciousness * unable to give consent

Design outcomes

Primary

MeasureTime frameDescription
Diagnosis is established on the positive signs of stroke highlighted on the CT scan or brain MRI according to the examination performed18 monthsProportion of patients with a diagnosis of stroke confirmed by cerebral radiology (MRI or scan according to examination) in the pre- and post-MRI groups.

Secondary

MeasureTime frameDescription
Number of CT and brain MRI requested by the emergency physician in the before / after groups18 monthsNumber of CT and brain MRI requested by the emergency physician in the before / after groups
Evaluate the usual management of vertigo and diplopia18 monthsEvaluate the usual management of vertigo and diplopia: number of CT and brain MRI requested by the emergency physician in the before / after groups; number of cerebral CT and MRI performed by the radiologist in the before / after groups
Evaluate the time of care18 monthsEvaluate the time of care: time of realization of the examination of radiology (scanner or brain MRI), delay of passage in emergencies
Rate of new emergency department visits for neurologicalthe month following initial emergency careRate of new emergency department visits for neurological reasons in the month following initial emergency care
Evaluate the irradiation rate18 monthsEvaluate the irradiation rate related to the initial radiological examination performed during emergency care
Evaluate the rate of new consultations in emergencies18 monthsEvaluate the rate of new consultations in emergencies for a neurological reason in the month following the initial care in emergencies, and the rate of new hospitalizations for the same reason

Countries

France

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 18, 2026