Alzheimer's drug put to the test against a different dementia
NCT ID NCT00200538
First seen Sep 14, 2026 · Last updated Sep 15, 2026 · Updated 1 time
Summary
Researchers are testing whether memantine, a drug already used for Alzheimer's disease, can ease symptoms or slow decline in people with frontotemporal dementia. The trial enrolls adults aged 45 to 75 with mild to moderate FTD and compares memantine against a placebo over one year. Neither participants nor doctors know who receives the drug, and the goal is to see whether it is effective and well tolerated.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- memantine, a drug that calms overactive brain signals and is already used in Alzheimer's disease
- What this could lead to
- If memantine helps, it could become one of the few options for easing frontotemporal dementia symptoms, a condition with no approved treatment.
- What could go wrong
- The trial is small and tests a drug borrowed from Alzheimer's research, so it may not work for a different form of dementia. Memantine can cause dizziness, headache, or confusion.
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
-
Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
-
52 people
The number who actually took part.
- Start date
-
Sep 2005
- 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.
- Ages
-
45 to 75 years
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Patients with FTD based on the criteria defined by the Lund and Manchester groups' consensus statement (revised in 1998), whose disease has been progressing during the last year. * MMSE score of 19 or higher * Men and women aged 45 to 75 years * Without speech, visuospatial, or episodic memory impairments Exclusion Criteria: * Age \> 76 years * Illiterate or misunderstanding patients * Patients with cancer, heart disease, lung disease, kidney disease (creatinine \> 200 mg/dL), or epilepsy
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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
-
Martine Vercelletto
Nantes, 44093, France
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