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

Stroke, Acute Clinical Trial

— CTP  

Official title:

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

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT04105257
• Other study ID #: CE19.072
• Status: Completed
• Phase: N/A
• Start date: October 20, 2019
• Est. completion date: October 4, 2022

Study information

• Verified date: December 2022
• Source: Centre hospitalier de l'Université de Montréal (CHUM)
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial 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.

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.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 7
• Est. completion date: October 4, 2022
• Est. primary completion date: October 4, 2022
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

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 .

Related Conditions & MeSH terms

• Stroke
• Stroke, Acute

Intervention

Diagnostic Test:
• All patients
Comparison of the results of the CTP with MRI

Locations

Country	Name	City	State
Canada	Centre hospitalier de l'Université de Montréal (CHUM)	Montréal	QC - Québec

Sponsors (1)

Lead Sponsor	Collaborator
Centre hospitalier de l'Université de Montréal (CHUM)

Country where clinical trial is conducted

Canada, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Sensibility	proportion of patients that are correctly identified as having a pseudo-stroke	: Immediately after the procedure (CTP scan/MRI)
Primary	Specificity	proportion of patient that are correctly identified as not having a pseudo-stroke	Immediately after the procedure (CTP scan/MRI)