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Neuromodulation and Language Acquisition (Project Stage Ia)
This study has been terminated.
Sponsored by: University Hospital Muenster
Information provided by: University Hospital Muenster
ClinicalTrials.gov Identifier: NCT00102284
  Purpose

The purpose of this study is to determine whether levodopa, pergolid, rivastigmine, or modafinil are effective in boosting semantic language acquisition in healthy subjects.


Condition Intervention Phase
Healthy
Drug: levodopa
Drug: rivastigmine
Drug: pergolid
Drug: modafinil
Phase IV

Drug Information available for: Modafinil Rivastigmine SDZ-ENA 713 Levodopa
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment, Efficacy Study
Official Title: Improved Language Acquisition Through Neuromodulation, Project Stage Ia

Further study details as provided by University Hospital Muenster:

Primary Outcome Measures:
  • Boost in language learning success through neuromodulation

Secondary Outcome Measures:
  • Stability of language learning success

Estimated Enrollment: 100
Study Start Date: March 2004
Estimated Study Completion Date: April 2005
Detailed Description:

Our prior work shows that d-amphetamine and the dopamine precursor levodopa markedly improve word learning success in healthy subjects. In this randomized, placebo-controlled, double-blind clinical trial, we probe whether a mixed d1/d2 dopamine agonist (pergolid) or cholinergic neuromodulation (rivastigmine) or a general centrally arousing substance (modafinil) will yield a learning enhancement comparable to using levodopa in healthy subjects.

Our results show that the dopamine agonist pergolide impaired learning in healthy subjects compared to placebo, whereas cholinergic neuromodulation had no effect.

  Eligibility

Ages Eligible for Study:   20 Years to 35 Years
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   Yes
Criteria

Inclusion Criteria:

  • Healthy subjects
  • 20-35 years old
  • Right handedness
  • Left language dominance (as assessed by functional transcranial Doppler ultrasonography [fTCD])

Exclusion Criteria:

  • Neurological/psychiatric/metabolic/cardiac disorders
  • Asthma
  • Known allergic reactions to one of the experimental drugs
  • Other drugs affecting the central nervous system
  • Leisure drug ingestion during the past 4 weeks (urine test)
  • Smoking cessation during the past 2 weeks
  • > 6 cups of coffee or energy drinks per day
  • > 10 cigarettes per day
  • > 50 grams of alcohol per day
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00102284

Locations
Germany, Nordrhein-Westfalen
Dept. of Neurology, University Hospital Muenster
Muenster, Nordrhein-Westfalen, Germany, 48129
Sponsors and Collaborators
University Hospital Muenster
Investigators
Study Director: Caterina Breitenstein, PhD Dept. of Neurology, University Hospital Muenster
Study Chair: Stefan Knecht, MD Dept. of Neurology, University Hospital Muenster
  More Information

Homepage of Dr. Breitenstein  This link exits the ClinicalTrials.gov site

Publications of Results:
Other Publications:
Study ID Numbers: KS-NEUROMOD_01, Stage Ia, IZKF Muenster: Kne3/074/04
Study First Received: January 26, 2005
Last Updated: September 7, 2006
ClinicalTrials.gov Identifier: NCT00102284  
Health Authority: Germany: Federal Institute for Drugs and Medical Devices

Keywords provided by University Hospital Muenster:
language acquisition
plasticity
stroke recovery
associative learning

Study placed in the following topic categories:
Levodopa
Rivastigmine
Cerebral Infarction
Stroke
Healthy
Modafinil

Additional relevant MeSH terms:
Cholinesterase Inhibitors
Neurotransmitter Agents
Molecular Mechanisms of Pharmacological Action
Therapeutic Uses
Physiological Effects of Drugs
Enzyme Inhibitors
Cholinergic Agents
Central Nervous System Agents
Protective Agents
Neuroprotective Agents
Pharmacologic Actions

ClinicalTrials.gov processed this record on January 15, 2009