Alzheimer's Disease 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 have been diagnosed with Alzheimer's disease based on specific medical guidelines (called IWG criteria)
- Your score on a standard memory and thinking test (called the MMSE) falls between 20 and 28, indicating mild to moderate difficulty
- Your brain scan or spinal fluid test has shown signs of a protein buildup linked to Alzheimer's disease (called amyloid)
- Your overall level of dementia, measured by a standard rating scale (CDR), is mild or less
- Your medical records show that your memory or thinking has been getting worse for more than six months
- You have a caregiver who lives with you or sees you regularly and is available to take part
- You live at home or in a care home that does not provide around-the-clock nursing care
- Your general health is good enough to take part in a six-month study
- Any medicines you take regularly have been the same for at least one month before the study begins
- You are not taking any medications that are not allowed in this trial
- You (and your caregiver) are willing and able to sign a consent form agreeing to take part
Who may not be able to join:
- You are unable to attend or complete the required check-up appointments at the start of the study
- You were hospitalised or had a change in your regular medicines in the month before or during the initial screening period
- You have been diagnosed with another type of dementia, such as Lewy body dementia, frontotemporal dementia, Huntington's disease, or a similar condition
- You have another brain or nervous system condition, such as Parkinson's disease or motor neurone disease (ALS)
- You have a condition causing sudden drops in blood pressure when standing (orthostatic hypotension) or problems with the body's automatic functions (confirm with trial site)
- You have had a significant stroke or have extensive damage to the white matter of the brain
- You have another serious brain condition, such as a tumour, severe head injury, or bleeding around the brain
- You have a history of epilepsy or seizures
- You have an infection, hormone problem, or other body-wide illness that affects the brain (for example, untreated low thyroid function or vitamin B12 deficiency)
- You currently have a diagnosis of severe depression, schizophrenia, or bipolar disorder
- You have a serious or unstable illness that could affect your ability to take part or be assessed safely
- You have a disability that would prevent you from completing all parts of the study, such as severe vision or hearing loss
- You regularly take strong painkiller medicines containing opioids
- You drink more than approximately one litre of beer or 500ml of wine per day, or have signs of alcohol or drug misuse
- In the opinion of the study doctor, there is any other reason you would not be suitable for the 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: Giacomo Koch, Prof., IRCCS Santa Lucia Foundation
Phone: +390651501181
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
integrated Alzheimer Disease Rating Scale (iADRS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 27 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.