Blood test may spot Alzheimer's early?
NCT ID NCT00647478
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This completed study measured levels of two substances (IGF-I and IGFBP-3) in the blood of 693 older adults: some with Alzheimer's disease, some with mild cognitive impairment, and some with normal memory. The goal was to see if these levels differ between groups and relate to thinking abilities. It is an observational study, not a treatment trial.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this could help identify biological markers for early detection or progression of Alzheimer's disease.
- What could go wrong
- This is an observational study, not a treatment trial. It only measures substances in the blood, so it cannot prove cause or lead directly to a therapy.
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.
- Participants
-
693 people
The number who actually took part.
- Started
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Oct 2007
- Finished
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Jul 2012
- Lead sponsor
-
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.
Who is studied
Ambulatory Elderly subjects
- Ages
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65 years and older
- Sex
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Anyone
- Healthy volunteers
-
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: Caucasian patients after a comprehensive geriatric assessment and giving informed written consent. \- In each arm : 1. elderly subjects with normal cognitive function, 2. patients with dementia of AD type (DSM-IV and NINCDS-ADRDA criteria), 3. patients with MCI (European Consortium on Alzheimer's Disease, EADC). Exclusion Criteria: Non AD dementia Major depression Use of anticholinesterase agent All diseases or major sensory deficits or any condition that might interfere with cognitive assessment and study objectives
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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.
Contacts and locations
Locations
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Broca Hospital Memory Clinic (CMRR)
Paris, Paris, 75013, France
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