Optimising 3D pH-Weighted CEST MRI in Acute Ischaemic Stroke (CEST in Stroke)
Primary Purpose
Stroke, Acute
Status
Recruiting
Phase
Not Applicable
Locations
United Kingdom
Study Type
Interventional
Intervention
3D CEST imaging
Sponsored by
About this trial
This is an interventional diagnostic trial for Stroke, Acute
Eligibility Criteria
Inclusion Criteria:
- Clinical diagnosis of acute anterior circulation ischaemic stroke
- Within 24 hours of symptom onset as defined by time since last known well
- Measurable neurological deficit (i.e. impairment of one or more of the following: language, motor function, cognition, gaze, vision, neglect)
- National Institutes of Health Stroke Scale (NIHSS) score of >= 10
- >= 18 years old
- Written informed consent from patient, legal representative or consultee
Exclusion Criteria:
- Any contraindication to MRI (e.g. cardiac pacemaker)
- Clinical diagnosis of posterior circulation ischaemic stroke
- NIHSS <10
- Evidence of intracranial haemorrhage or significant non-stroke intracranial pathology (including CNS [central nervous system] neoplasm) on CT
- Seizure at onset of symptoms unless CT identifies positive evidence of significant brain ischaemia (e.g. arterial occlusion, early ischaemic change)
- Planned or anticipated intravenous thrombolysis or endovascular re-perfusion strategies
- Pregnancy
- Known allergy to MRI contrast agent
Sites / Locations
- King's College HospitalRecruiting
Arms of the Study
Arm 1
Arm Type
Other
Arm Label
CEST imaging performed
Arm Description
CEST imaging will be performed (15 min): Axial 3D volume acquisition at 3.5 mm isotropic voxel size, 20-30 offset frequencies, plus Axial 3D T1w and T2w map at same resolution for use in CEST quantification. A routine stroke MRI protocol will also be performed (10 min): Axial T2w; Axial DWI and ADC (apparent diffusion coefficient) using accelerated multi-band sequence; Axial T2w* or SWI (susceptibility weighted imaging); and dynamic susceptibility contrast-enhanced (DSC) perfusion imaging following contrast agent administration (5 min, provided Radiology Department protocols allow DSC (e.g. no renal impairment)).
Outcomes
Primary Outcome Measures
Technical feasibility of 3D CEST imaging in acute stroke: Percentage of patients where acquisition of a comprehensive raw CEST dataset can be performed over the human brain
Percentage of patients where acquisition of a comprehensive raw CEST dataset can be performed over the human brain
Technical feasibility of 3D CEST imaging in acute stroke: Percentage of patients with quantitative maps of different CEST contrasts produced including APT, NOE, and pH-weighted
Percentage of patients with quantitative maps of different CEST contrasts produced including APT, NOE, and pH-weighted
Technical feasibility of 3D CEST imaging in acute stroke: Signal-to-noise ratio on the CEST contrasts determined: with and without motion
Signal-to-noise ratio on the CEST contrasts determined: with and without motion
Secondary Outcome Measures
Clinical feasibility: Number of patients recruited per month (determined at completion of study)
Number of patients recruited per month (determined at completion of study)
Clinical feasibility: Patients tolerating full scan protocol per month
Number of patients tolerating full scan protocol per month
Dice score of abnormality seen on CEST contrast & routine stroke sequences
CEST contrast & perfusion imaging (including PWI-DWI mismatch)
Full Information
NCT ID
NCT04282330
First Posted
February 10, 2020
Last Updated
April 4, 2022
Sponsor
King's College Hospital NHS Trust
Collaborators
King's College London
1. Study Identification
Unique Protocol Identification Number
NCT04282330
Brief Title
Optimising 3D pH-Weighted CEST MRI in Acute Ischaemic Stroke (CEST in Stroke)
Official Title
Optimising 3D pH-Weighted CEST MRI in Acute Ischaemic Stroke (CEST in Stroke)
Study Type
Interventional
2. Study Status
Record Verification Date
April 2022
Overall Recruitment Status
Recruiting
Study Start Date
June 13, 2018 (Actual)
Primary Completion Date
April 30, 2023 (Anticipated)
Study Completion Date
April 30, 2023 (Anticipated)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor
Name of the Sponsor
King's College Hospital NHS Trust
Collaborators
King's College London
4. Oversight
Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No
Data Monitoring Committee
No
5. Study Description
Brief Summary
CEST in Stroke is an observational magnetic resonance imaging (MRI) study in acute ischaemic stroke patients. Ischaemic stokes are the most common type of stroke and occur when a blood clot blocks the flow of blood and oxygen your brain needs. This can lead to cellular death (infarction) so the quicker a stroke is diagnosed and treated, the better a patient's recovery is likely to be.
The purpose of this study is to determine the technical feasibility of a new MRI technique known as Chemical Exchange Saturation Transfer (CEST) imaging for assessing the extent of potentially salvageable brain tissue (penumbra) around an area of infarction. CEST imaging works by looking at the chemicals in the brain cells. The chemicals may change when cells are affected by stroke. Stroke patients are not normally treated with with clotbusting drugs or clot-retrieving devices if they arrive at hospital many hours after the stroke because treatment may not help and in some cases it may cause more harm than good. However, the new MRI technique could detect those stroke patients who arrive at hospital many hours after the stroke but still have salvageable brain - in these cases it would be helpful to treat these patients and therefore stop those cells from dying.
However, there are several technical issues that need to be addressed before CEST can be adopted as a routine clinical assessment. CEST in Stroke hopes to address these issues by using an alternate MRI sequence capable of acquiring CEST data over a large portion of the brain in approximately in 10 minutes.
The overall aim of study is to determine the feasibility of CEST imaging for assessing the extent of penumbra, in order to determine which patients may benefit from re-perfusion interventions who would otherwise not be eligible. If the study is successful, further research will be implemented to help clinical decision making in stroke patients who present outside of conventional time windows.
Detailed Description
CEST in Stroke is an observational magnetic resonance imaging (MRI) study in acute ischaemic stroke patients. Ischaemic stokes are the most common type of stroke and occur when a blood clot blocks the flow of blood and oxygen your brain needs. This can lead to cellular death (infarction) so the quicker a stroke is diagnosed and treated, the better a patient's recovery is likely to be.
The purpose of this study is to determine the technical feasibility of a new MRI technique known as Chemical Exchange Saturation Transfer (CEST) imaging for assessing the extent of potentially salvageable brain tissue (penumbra) around an area of infarction. CEST imaging works by looking at the chemicals in the brain cells. The chemicals may change when cells are affected by stroke. Stroke patients are not normally treated with with clotbusting drugs or clot-retrieving devices if they arrive at hospital many hours after the stroke because treatment may not help and in some cases it may cause more harm than good. However, the new MRI technique could detect those stroke patients who arrive at hospital many hours after the stroke but still have salvageable brain - in these cases it would be helpful to treat these patients and therefore stop those cells from dying.
However, there are several technical issues that need to be addressed before CEST can be adopted as a routine clinical assessment. CEST in Stroke hopes to address these issues by using an alternate MRI sequence capable of acquiring CEST data over a large portion of the brain in approximately in 10 minutes.
The overall aim of study is to determine the feasibility of CEST imaging for assessing the extent of penumbra, in order to determine which patients may benefit from re-perfusion interventions who would otherwise not be eligible. If the study is successful, further research will be implemented to help clinical decision making in stroke patients who present outside of conventional time windows.
Eligible participants (or a consultee) will be approached upon admission in A&E or on the Hyper Acute Stroke Unit within 24 hours of onset. The study will be described in detail and an information sheet provided. After being given sufficient time to consider participation, the participant or their consultee will be asked to complete a consent form. They will be given a copy of the consent form and information sheet for their records.
A one off study visit will then take place. This will entail a 30 minute MRI scan in the King's College Hospital Clinical Research Facility. In addition, a brief neurological assessment (routine examination for all stroke patients) will also be performed and the following information collected: demographics, past medical history and any local laboratory results. The participant's clinical details will be recorded on a case report form (CRF). Any clinical information not provided by the participant will be completed using the patient's medical notes.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Stroke, Acute
7. Study Design
Primary Purpose
Diagnostic
Study Phase
Not Applicable
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
N/A
Enrollment
28 (Anticipated)
8. Arms, Groups, and Interventions
Arm Title
CEST imaging performed
Arm Type
Other
Arm Description
CEST imaging will be performed (15 min): Axial 3D volume acquisition at 3.5 mm isotropic voxel size, 20-30 offset frequencies, plus Axial 3D T1w and T2w map at same resolution for use in CEST quantification. A routine stroke MRI protocol will also be performed (10 min): Axial T2w; Axial DWI and ADC (apparent diffusion coefficient) using accelerated multi-band sequence; Axial T2w* or SWI (susceptibility weighted imaging); and dynamic susceptibility contrast-enhanced (DSC) perfusion imaging following contrast agent administration (5 min, provided Radiology Department protocols allow DSC (e.g. no renal impairment)).
Intervention Type
Diagnostic Test
Intervention Name(s)
3D CEST imaging
Intervention Description
Chemical Exchange Saturation Transfer (CEST) is an emerging MRI technique that can acquire multiple endogenous contrasts to probe cerebral metabolism.
Primary Outcome Measure Information:
Title
Technical feasibility of 3D CEST imaging in acute stroke: Percentage of patients where acquisition of a comprehensive raw CEST dataset can be performed over the human brain
Description
Percentage of patients where acquisition of a comprehensive raw CEST dataset can be performed over the human brain
Time Frame
Within 24 hours of ictus
Title
Technical feasibility of 3D CEST imaging in acute stroke: Percentage of patients with quantitative maps of different CEST contrasts produced including APT, NOE, and pH-weighted
Description
Percentage of patients with quantitative maps of different CEST contrasts produced including APT, NOE, and pH-weighted
Time Frame
Within 24 hours of ictus
Title
Technical feasibility of 3D CEST imaging in acute stroke: Signal-to-noise ratio on the CEST contrasts determined: with and without motion
Description
Signal-to-noise ratio on the CEST contrasts determined: with and without motion
Time Frame
Within 24 hours of ictus
Secondary Outcome Measure Information:
Title
Clinical feasibility: Number of patients recruited per month (determined at completion of study)
Description
Number of patients recruited per month (determined at completion of study)
Time Frame
Within 24 hours of ictus
Title
Clinical feasibility: Patients tolerating full scan protocol per month
Description
Number of patients tolerating full scan protocol per month
Time Frame
Within 24 hours of ictus
Title
Dice score of abnormality seen on CEST contrast & routine stroke sequences
Description
CEST contrast & perfusion imaging (including PWI-DWI mismatch)
Time Frame
Within 24 hours of ictus
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Clinical diagnosis of acute anterior circulation ischaemic stroke
Within 24 hours of symptom onset as defined by time since last known well
Measurable neurological deficit (i.e. impairment of one or more of the following: language, motor function, cognition, gaze, vision, neglect)
National Institutes of Health Stroke Scale (NIHSS) score of >= 10
>= 18 years old
Written informed consent from patient, legal representative or consultee
Exclusion Criteria:
Any contraindication to MRI (e.g. cardiac pacemaker)
Clinical diagnosis of posterior circulation ischaemic stroke
NIHSS <10
Evidence of intracranial haemorrhage or significant non-stroke intracranial pathology (including CNS [central nervous system] neoplasm) on CT
Seizure at onset of symptoms unless CT identifies positive evidence of significant brain ischaemia (e.g. arterial occlusion, early ischaemic change)
Planned or anticipated intravenous thrombolysis or endovascular re-perfusion strategies
Pregnancy
Known allergy to MRI contrast agent
Facility Information:
Facility Name
King's College Hospital
City
London
ZIP/Postal Code
SE5 9RS
Country
United Kingdom
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Jonnie Aeron-Thomas, MSc
Phone
0203 299 900
Ext
7506
Email
j.aeron-thomas@nhs.net
12. IPD Sharing Statement
Plan to Share IPD
No
Learn more about this trial
Optimising 3D pH-Weighted CEST MRI in Acute Ischaemic Stroke (CEST in Stroke)
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