Stroke Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- People who are 18 years of age or older
- People who have been assessed as needing a transcatheter aortic valve replacement (a minimally invasive procedure to replace a heart valve)
- People who are willing to attend follow-up appointments as outlined in the study plan
- People who have been fully informed about the study and have agreed to take part by signing a consent form
Who may not be able to join:
- People whose heart valve procedure is planned to be done through any access point other than the groin (for example, through the shoulder, armpit, chest wall, main artery, neck, or abdomen)
- People whose body structure makes it unsafe to use the study device
- People who are currently using or planning to use another experimental drug or medical device during the study period
- People who have had or are planning to have another heart or blood vessel procedure within 10 days before the valve procedure, or within 30 days after it
- People who have a bleeding disorder that is not under control
- People who are pregnant, as confirmed by a positive pregnancy test
- People whose body size or weight makes it not possible to fit safely inside an MRI scanner
- People who cannot have an MRI scan — for example, those who have a pacemaker, defibrillator, metal implants in certain areas of the body, or metal fragments near the brain or eye
- People who are considered at high risk of needing a permanent pacemaker after the procedure, such as those with certain pre-existing electrical problems in the heart (confirm with trial site)
- People who already have or are planned to receive a pacemaker or defibrillator within the first 3 days after the procedure
- People who experience severe anxiety in enclosed spaces (claustrophobia) that would prevent them from undergoing an MRI scan
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Robert Gooley, MD, Monash Health
Phone: +13033252945
Australian sites
+6137511 1500
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
1 site(s) in Australia. Confirm current status and contact details directly with the trial site.
Primary endpoints
Primary Endpoint; Primary Safety Endpoints
Can't join this trial?
Data last synced from ClinicalTrials.gov: 12 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.