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Evaluation of Diagnostic Performance of Cerebral Perfusion Scans in Pseudo-Stroke

Evaluation of Diagnostic Performance of Cerebral Perfusion Scans in Pseudo-Stroke: Exploratory Study of Diagnostic Performance

Status
Completed
Phases
NA
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT04105257
Acronym
CTP
Enrollment
7
Registered
2019-09-26
Start date
2019-10-20
Completion date
2022-10-04
Last updated
2022-12-12

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

Conditions

Stroke, Acute

Brief summary

When a patient is received with the context of acute stroke, they undergo a fast neurological evaluation and obtain a basic appraisal composed of a non-contrast endovascular cerebral scan and an angiography scan of intracranial blood vessels and the neck. Once the structural lesion (hemorrhage, tumor, etc.) is absent, signs of early infracts and confirmed acute intracranial arterial occlusion, the possibility of a pseudo-stroke dwells in the differential diagnostic. Certain characteristics of history and clinical evaluation create sufficient doubt to evoke the possibility of a pseudo-stroke. In fact, this population is mostly female and the cardiovascular risk factors are less prevalent in this group than for the group of stroke victims. It is on average the youngest and presents a less severe deficit. For the rest, medical antecedents often help to evoke a diagnosis of pseudo-stroke.

Detailed description

With this study, the investigators wish to evaluate the diagnostic value of two additional radiological examinations: 1. Computed tomography perfusion (CTP) imaging to evaluate blood flow in the brain; 2. Imaging by magnetic resonance (MRI) of the brain to detect lesions from a cerebral vascular accident (stroke) not visible on standard imaging of the brain. The proposed additional examinations (CTP and MRI) are tests that are currently used at the CHUM. Those are not experimental tests. These tests are commonly used when doctors wants a further investigation to clarify the cause of the neurological symptoms. These tests are usually done in a semi-urgent or non-urgent situations. In the present study they will be done urgently. The investigators wish to determine if obtaining these additional tests in emergency will change the decision of whether to administer the drug (thrombolysis). The investigators want to determine whether one imaging test is sufficient or if both exams are needed to help clinical decision-making. Please note that urgent access to perfusion CT and brain MRI is not considered routine care, since the value of these additional tests has yet to be demonstrated.

Interventions

DIAGNOSTIC_TESTAll patients

Comparison of the results of the CTP with MRI

Sponsors

Centre hospitalier de l'Université de Montréal (CHUM)
Lead SponsorOTHER

Study design

Allocation
NA
Intervention model
SINGLE_GROUP
Primary purpose
DIAGNOSTIC
Masking
NONE

Eligibility

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

Inclusion criteria

1. Admission at CHUM for acute neurological deficit \<4,5h (since the onset of symptoms) 2. Potential candidate for an intravenous thrombolysis 3. Cerebral angioscan performed at CHUM at the time of admission 4. Age ≥ 18 years 5. Observed period from September 2019 à June 2020

Exclusion criteria

1. Contraindication to intravenous thrombolysis according to the doctor in charge of treatment; 2. Indication of a thrombectomy; 3. Incomplete exam or exam of insufficient technical quality for a reliable radiological interpretation; 4. Contraindication against MRI .

Design outcomes

Primary

MeasureTime frameDescription
Sensibility: Immediately after the procedure (CTP scan/MRI)proportion of patients that are correctly identified as having a pseudo-stroke
SpecificityImmediately after the procedure (CTP scan/MRI)proportion of patient that are correctly identified as not having a pseudo-stroke

Countries

Canada

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026