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:
- People who are willing and able to sign the official consent form approved by the relevant authorities.
- People who are already enrolled in the ALFA project (Study 45-65 FPM/2012).
- People whose brain MRI scan does not show any findings that would otherwise rule them out of the trial.
- People whose memory and thinking abilities fall within the normal range, based on two standard tests (a general thinking test scoring 26 or above, and a word-finding test scoring 12 or above for naming animals).
- People who score 0 on a standard dementia rating scale, meaning no signs of dementia have been detected.
- People who have a good understanding of the language used in the study and are able to read and write.
- Female participants who have gone through menopause, or who have a negative pregnancy test at the time of the brain imaging scan.
Who may not be able to join:
- People who already have a diagnosed problem with memory or thinking (cognitive impairment).
- People who have been diagnosed with certain mental health conditions, including major depression, generalised anxiety disorder, schizophrenia, or bipolar disorder.
- People who have significant vision or hearing difficulties.
- People with a history of brain infection (encephalitis), stroke, or seizures (not including childhood febrile convulsions caused by fever).
- People whose MRI scan shows serious blood vessel disease in the brain (such as multiple strokes) or a brain tumour.
- People for whom an MRI scan is not safe or possible — for example, due to metal implants in the body — or who have a strong fear of enclosed spaces that would prevent them from completing the scan, as assessed by the doctor at the trial site.
- People who have taken part in another clinical trial involving an experimental medication within the 30 days before screening, or who have received a radioactive substance within a specific timeframe before this study's imaging procedure (confirm with trial site for exact timing details).
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: Jose Luis Molinuevo, MD, PhD, Scientific Director
Phone: 933160990
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
Prevalence of a positive 18F-Flutemetamol scan
Can't join this trial?
Data last synced from ClinicalTrials.gov: 21 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.