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MRI Imaging Techniques for Brain Arteriovenous Malformations
N/A
Recruiting
Led By Daniela Iancu, MD
Research Sponsored by Ottawa Hospital Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Brain AVMs previously diagnosed with either CT Angiography, MRI or catheter angiography
mRS <=2
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 24 months
Awards & highlights
Study Summary
This trial is studying how well endovascular embolization works compared to surgery in treating brain arteriovenous malformations.
Who is the study for?
This trial is for adults over 18 with brain arteriovenous malformations (AVMs) visible on MRI, specifically where the abnormal tangle of arteries measures more than 1 cm. Participants must be able to give informed consent, have a minor or no disability from their condition (mRS <=2), and are scheduled for cerebral catheter angiography. Those with non-MRI compatible implants, severe claustrophobia, kidney issues (GFR < 60 ml/min), or contrast allergies cannot join.Check my eligibility
What is being tested?
The study tests advanced MRI techniques like susceptibility-weighted imaging and time-resolved magnetic resonance angiography in patients with brain AVMs. These methods aim to provide detailed images of blood flow in the brain to help plan treatments that prevent bleeding or other neurological symptoms without harming normal brain function.See study design
What are the potential side effects?
Since this trial involves MRI scans which are generally safe and non-invasive, side effects are rare but may include discomfort from lying still during the scan or reactions to contrast agents used if applicable.
Eligibility Criteria
Inclusion Criteria
You may be eligible if you check “Yes” for the criteria belowSelect...
My brain AVM was confirmed by a CT, MRI, or catheter angiography.
Select...
I can carry out all my usual duties with minimal help.
Select...
I am scheduled for a special brain scan to check for abnormal blood vessels.
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I am older than 18 years.
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 24 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~24 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Angiogram
Trial Design
1Treatment groups
Experimental Treatment
Group I: MRI perfusion imagingExperimental Treatment1 Intervention
SWAN imaging on the GE 3 T has been attempted but the preliminary evidence suggest that the images are of low resolution and difficult to interpret. Similarly, early experience with TRMRA suggest poor spatial and temporal resolution using the standard "out-of-the-box" protocols.
Thus, there is a significant opportunity to improve SWAN and TRMRA, to evaluate the evolution of progressive obliteration of the AVM nidus. Specifically, this is attractive for brain AVMs that are treated with radiosurgery as MRI is required for clinical grounds for treatment planning purposes.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
MRI perfusion imaging
2018
N/A
~40
Find a Location
Who is running the clinical trial?
Ottawa Hospital Research InstituteLead Sponsor
561 Previous Clinical Trials
2,785,482 Total Patients Enrolled
Daniela Iancu, MDPrincipal InvestigatorOttawa Hospital Research Institute
2 Previous Clinical Trials
340 Total Patients Enrolled
Howard Lesiuk, MDPrincipal InvestigatorOttawa Hospital Research Institute
Media Library
Eligibility Criteria:
This trial includes the following eligibility criteria:- I am scheduled for a brain scan before my angiography.I can carry out all my usual duties with minimal help.You have a large brain AVM that can be seen on an MRI scan.I cannot have contrast due to poor kidney function or an allergy.I am scheduled for a special brain scan to check for abnormal blood vessels.I am older than 18 years.You are unable to have an MRI due to having a non-MRI compatible implant or severe claustrophobia.My brain AVM was confirmed by a CT, MRI, or catheter angiography.
Research Study Groups:
This trial has the following groups:- Group 1: MRI perfusion imaging
Awards:
This trial has 1 awards, including:- No Placebo-Only Group - All patients enrolled in this study will receive some form of active treatment.
Timeline:
This trial has the following timeline:- Screening: It may take up to 3 Weeks to process to see if you qualify in this trial.
- Treatment: The duration you will receive the treatment varies.
- Follow Ups: You may be asked to continue sharing information regarding the trial for 6 Months after you stop receiving the treatment.
Frequently Asked Questions
These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.
Is recruitment for this clinical trial still active?
"Affirmative. According to the information posted on clinicaltrials.gov, this medical trial is looking for 12 patients from a single location and was first shared in March 2020 before being updated recently in June 2022."
Answered by AI
How many participants are permitted to join this clinical research project?
"That is correct. Information found on clinicaltrials.gov indicates that this medical trail, which was initially posted on March 1st 2020, continues to search for participants. The research requires 12 patients from 1 centre to be recruited."
Answered by AI
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