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:
For patients:
- People who have had a stroke or a transient ischaemic attack (a brief, stroke-like episode) that meets certain medical severity criteria, as assessed by the trial site
- People whose level of disability after stroke or TIA is mild (a score of 2 or less on a standard disability scale used by doctors)
- People the investigator believes are able to follow all the requirements of the study
- People who are able to understand and sign a consent form
- People who score 12 or higher on a standard fatigue questionnaire in the "general fatigue" section
For healthy participants (comparison group):
- People who are in good health
- People whose age and sex match those of the patient group, as determined by the trial site
- People the investigator believes are able to follow all the requirements of the study
- People who are able to understand and sign a consent form
Who may not be able to join:
For patients:
- People who do not meet the MRI research safety requirements set by the DRCMR (the research centre running the trial) (confirm with trial site)
- People who are pregnant or breastfeeding — women under 55 may be offered a urine pregnancy test at the trial site
- People with a significant ongoing medical condition, such as anaemia, diabetes, thyroid problems, heart or blood vessel disease, or an imbalance of salts and minerals in the body
- People currently taking Ritalin (methylphenidate) or modafinil
- People with a known severe cancer that is not under control
- People with a known addiction to drugs or alcohol
- People whose tiredness is considered by the investigator to be caused by side effects of medication
- People who weigh more than 130 kg
- People who do not wish to be told about any unexpected health findings discovered during the study
For healthy participants (comparison group):
- People who do not meet the MRI research safety requirements set by the DRCMR (confirm with trial site)
- People who are pregnant or breastfeeding — women under 55 may be offered a urine pregnancy test at the trial site
- People with a significant ongoing medical condition, such as anaemia, diabetes, thyroid problems, heart or blood vessel disease, or an imbalance of salts and minerals in the body
- People who have had an infection (such as a urinary tract infection, flu, or pneumonia) in the past three weeks
- People with any known cancer
- People with a known addiction to drugs or alcohol
- People whose tiredness is considered to be caused by side effects of medication
- People who weigh more than 130 kg
- People who do not wish to be told about any unexpected health findings discovered during the study
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: Tim B. Dyrby, Professor, Danish Research Centre for Magnetic Resonance
Phone: 38626446
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
Microstructural changes in the brain network, and its correlate with functional deficits in patients with minor stroke or TIA.
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.