Brain scans track Alzheimer's clues over decades
NCT ID NCT00950430
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This study uses special brain scans (PET imaging) to measure amyloid buildup—a protein linked to Alzheimer's—in healthy older adults, people with mild memory problems, and those with dementia. Participants receive scans every 2-3 years for up to 20 years to see how amyloid changes over time and relates to memory decline. The goal is to improve early diagnosis and understanding of Alzheimer's and related dementias.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Pittsburgh Compound B (C-11 PiB) and F-18 FDG
- What this could lead to
- If successful, this could lead to better early detection and tracking of Alzheimer's and other dementias, helping doctors diagnose and monitor these diseases more accurately.
- What could go wrong
- This is an observational imaging study, not a treatment trial. It may not directly improve patient outcomes, and results may take many years to yield practical benefits.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
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About 8,000 people
The number the study aims to enrol. It can still change while the study runs.
- Start date
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Apr 2008
- Expected to finish
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Jun 2027
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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30 to 100 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Age 30-100 * Subjects who have completed or are scheduled to undergo the neurological evaluation procedures in the Mayo Clinic Study of Aging, Mayo ADRC, or Mayo neurodegenerative disease clinics. Exclusion Criteria: * Subjects unable to lie down without moving for 10 minutes * Women who are pregnant or cannot stop breast feeding for 24 hours at the time of scanning * Claustrophobic patients unable to tolerate the scans * Standard safety exclusionary criteria for MRI such as metallic foreign bodies, pacemaker, etc.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Mayo Clinic
Rochester, Minnesota, 55905, United States
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