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Dopaminergic Enhancement of Learning and Memory in Healthy Adults and Patients With Dementia/Mild Cognitive Impairment

Dopaminergic Enhancement of Learning and Memory (LL_001, Project on Dementia/MCI)

Status
UNKNOWN
Phases
Phase 4
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00306124
Enrollment
120
Registered
2006-03-22
Start date
2006-01-31
Completion date
2008-03-31
Last updated
2007-10-25

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Alzheimer's Disease, Healthy, Mild Cognitive Impairment

Keywords

Dementia, Mild Cognitive Impairment, MCI, levodopa, learning, enhancement

Brief summary

This study aims to determine whether levodopa is effective in boosting learning and memory in healthy subjects and patients with dementia or Mild Cognitive Impairment. We also examine in healthy subjects using functional magnetic resonance imaging which brain regions mediate improved learning after levodopa administration.

Detailed description

Prior work of our group shows that the dopamine precursor levodopa markedly improves word learning success in healthy subjects. In this randomized, placebo-controlled, double-blind trial, we probe whether administration of levodopa improves learning performance as compared to placebo administration on neuropsychological tests and in an associative learning paradigm. We postulate that levodopa improves learning success and memory performance in healthy subjects, while the effect in patients with dementia or Mild Cognitive Impairment might depend on other factors, including severity of memory impairment.

Interventions

DRUGLevodopa

Sponsors

University Hospital Muenster
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
TREATMENT
Masking
DOUBLE

Eligibility

Sex/Gender
ALL
Age
18 Years to 90 Years
Healthy volunteers
Yes

Inclusion criteria

for patients with dementia: * Patients: clinical diagnosis of AD or mild cognitive impairment * primary language German

Exclusion criteria

for healthy subjects and patients with dementia/MCI: * Known allergy to levodopa or tetrazine * History of medication/drug abuse * Acute nicotine withdrawal or \> 15 cigarettes per day * \> 6 cups/glasses of coffee, caffeine drinks or energy drinks per day * \> 50 grams of alcohol per day * Severe hypertonia (systole \>160 mm Hg) * Severe arteriosclerosis * Diabetes, asthma, or glaucoma * Severe hearing disability * no focal brain lesions * Premorbid depression or psychosis * Medication with dopamine agonists or antagonists * Parkinsonian symptoms

Design outcomes

Primary

MeasureTime frame
Cognitive performance assessed by neuropsychological tests and learning paradigms under placebo and levodopa in healthy subjects and patients with dementia or Mild Cognitive Impairment.
Brain activity pattern during learning under levodopa as compared to placebo in healthy subjects.

Secondary

MeasureTime frame
Long-term stability of learning performance after 1 month in healthy subjects.

Countries

Germany

Contacts

Primary ContactBernward Winter, MSc
bwinter@uni-muenster.de+49-251-83

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026