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:
- You are 50 years of age or older
- You have recently had an ischemic stroke (caused by a blockage) within the last 72 hours, confirmed by a specific type of brain scan called an MRI
- The stroke affected either the outer layer of the brain (cortex) or a deeper area within the brain
- You are able and willing to sign a consent form before joining the study
- You are willing to attend follow-up appointments and take part in study assessments
Who may not be able to join:
- You are unable or unwilling to sign a written consent form
- You have had a previous stroke, multiple past strokes, or strokes affecting the back part of the brain (brain stem or cerebellum)
- You have a known condition affecting the brain or nervous system other than this stroke
- You have received treatments that affect the immune system in the 3 months before your stroke
- You have a long-term inflammatory condition (such as rheumatoid arthritis or similar) (confirm with trial site)
- You had an infection in the 7 days before your stroke
- You have a serious illness, such as advanced cancer, that may make follow-up visits difficult
- You have a medical device or condition that prevents you from having an MRI or PET scan (for example, a pacemaker, certain metal clips, or a cochlear implant)
- You have already had significant radiation exposure this year (more than 10mSv) (confirm with trial site)
- You are currently pregnant or breastfeeding
- You are already taking part in another clinical trial
⚠️ 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: Martin Dichgans, Prof., LMU Munich
Phone: +49 4400
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
Primary endpoints
microglia activation in patients with acute stroke; microglia activation in patients with acute stroke; functional outcome in patients after acute ischemic stroke; functional outcome in patients after acute ischemic stroke; functional outcome in patients after acute ischemic stroke; functional outcome in patients after acute ischemic stroke; cognitive outcome in patients after acute ischemic stroke; cognitive outcome in patients after acute ischemic stroke; cognitive outcome in patients after acute ischemic stroke; cognitive outcome in patients after acute ischemic stroke
Can't join this trial?
Data last synced from ClinicalTrials.gov: 14 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.