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Influence of G-CSF and EPO on Associative Learning and Motor Skills
This study has been completed.
First Received: March 1, 2006   Last Updated: April 22, 2009   History of Changes
Sponsored by: University Hospital Muenster
Information provided by: University Hospital Muenster
ClinicalTrials.gov Identifier: NCT00298597
  Purpose

In the study we want to prove whether the subcutaneous application of granulocyte-stimulating factor (G-CSF) and erythropoetin (EPO) influence associative learning and/or motor skills of patients, who suffer from chronic stroke or amyotrophic lateral sclerosis. The study hypothesis is that G-CSF and EPO improve associative learning and/or motor skills.


Condition Intervention Phase
Chronic Stroke
Amyotrophic Lateral Sclerosis
Drug: granulocyte - colony stimulating factor (G-CSF)
Drug: erythropoetin (EPO)
Phase II

Genetics Home Reference related topics: amyotrophic lateral sclerosis
MedlinePlus related topics: Amyotrophic Lateral Sclerosis
Drug Information available for: Granulocyte colony-stimulating factor
U.S. FDA Resources
Study Type: Interventional
Study Design: Treatment, Randomized, Double-Blind, Placebo Control, Parallel Assignment
Official Title: Influence of G-CSF and EPO on Associative Learning and Motor Skills

Further study details as provided by University Hospital Muenster:

Primary Outcome Measures:
  • Learning success in a word learning model
  • Response time in motor function tests

Secondary Outcome Measures:
  • Response time in a word learning model
  • Total time and number of keystrokes in motor function tests

Estimated Enrollment: 180
Study Start Date: March 2006
Study Completion Date: March 2009
Primary Completion Date: March 2009 (Final data collection date for primary outcome measure)
  Eligibility

Ages Eligible for Study:   18 Years and older
Genders Eligible for Study:   Both
Accepts Healthy Volunteers:   No
Criteria

Inclusion Criteria:

  • Diagnosis of chronic stroke or amyotrophic lateral sclerosis

Exclusion Criteria:

  • leucocytes > 10000/µl
  • hematocrit > 48%
  • thrombocytes < 150000/µl
  • severe rheumatoid arthritis
  • severe infection
  • severe liver or renal failure
  • severe arterial hypertension
  • recurrent thromboembolic events
  • severe coronary heart disease
  • myocardial infarction
  • malignant tumor
  • leukemia
  • peripheral arterial occlusion disease
  Contacts and Locations
Please refer to this study by its ClinicalTrials.gov identifier: NCT00298597

Locations
Germany, Nordrhein-Westfalen
Department of neurology, University Hospital of Muenster
Muenster, Nordrhein-Westfalen, Germany, D-48149
Sponsors and Collaborators
University Hospital Muenster
Investigators
Principal Investigator: Wolf Rüdiger Schäbitz, MD Department of Neurology, University Hospital of Muenster, Germany
  More Information

Publications:
Study ID Numbers: GCSFEPO_01, EudraCT Number 2005-001113-18
Study First Received: March 1, 2006
Last Updated: April 22, 2009
ClinicalTrials.gov Identifier: NCT00298597     History of Changes
Health Authority: Germany: Federal Institute for Drugs and Medical Devices

Study placed in the following topic categories:
Epoetin Alfa
Lou Gehrig's Disease
Neuromuscular Diseases
Spinal Cord Diseases
Cerebral Infarction
Amyotrophic Lateral Sclerosis
Stroke
Central Nervous System Diseases
Sclerosis
Neurodegenerative Diseases
Degenerative Motor System Disease
Motor Neuron Disease

Additional relevant MeSH terms:
Pathologic Processes
Neuromuscular Diseases
Spinal Cord Diseases
Amyotrophic Lateral Sclerosis
Nervous System Diseases
Central Nervous System Diseases
Sclerosis
Neurodegenerative Diseases
Motor Neuron Disease

ClinicalTrials.gov processed this record on May 06, 2009