- ICH GCP
- US Clinical Trials Registry
- Clinical Trial NCT01730274
Cerebellum - Cognitive Outcome and Functional Connectivity
Cerebellar Tumors of Childhood - Impact on Cognition and Functional Connectivity
Aim: To investigate the effect of cerebellar tumor surgery on the resting state functional connectivity level in higher order cognition networks known to interact with the cerebellum. Furthermore, to correlate the connectivity level of these networks with the neuropsychological performance and functional outcome of the patients.
The investigator's hypothesis is that the functional connectivity of various cognition networks in the cerebrum as assessed by resting-state functional magnetic resonance imaging can be impaired after cerebellar tumor surgery and can be correlated with the neuropsychological performance. The effect of surgery on the cognition networks and the neuropsychological performance is dependent on the tumor location within the cerebellum. Such a correlation seems feasible as functional connectivity analysis could be correlated with the neuropsychological impairment in various neuropsychiatric disorders. Furthermore, investigators were able to depict the maturation of the functional connectivity networks in parallel to the neurocognitive development in childhood
Study Overview
Status
Conditions
Study Type
Enrollment (Actual)
Contacts and Locations
Study Locations
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Vienna, Austria, 1090
- MUV, Department of Neurosurgery
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Participation Criteria
Eligibility Criteria
Ages Eligible for Study
Accepts Healthy Volunteers
Genders Eligible for Study
Sampling Method
Study Population
Description
Inclusion Criteria:
• Male or female patients aged > 15 yrs
- Age at surgery between 1 yrs - 12 yrs
- Compliance (the patients have to be able to lay motionless in a 3 Tesla MR scanner and to cooperate with the examiner during the examination)
- Signed informed consent from the patient and/or the parents
Exclusion Criteria:
• Patients with Neurofibromatosis 1
- Severe visual or auditory impairment
- Cerebrospinal fluid shunt device
- Prior radiotherapy or chemotherapy
- Contraindications to MRI
Study Plan
How is the study designed?
Design Details
Cohorts and Interventions
Group / Cohort |
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patients
children operated on a cerebellar tumor
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healthy subjects
healthy volunteers
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What is the study measuring?
Primary Outcome Measures
Outcome Measure |
Time Frame |
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neuropsychological assessment
Time Frame: up to 24 months
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up to 24 months
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Collaborators and Investigators
Sponsor
Investigators
- Principal Investigator: Christian Dorfer, MD, MUV, Department of Neurosurgery
Study record dates
Study Major Dates
Study Start
Primary Completion (Actual)
Study Completion (Actual)
Study Registration Dates
First Submitted
First Submitted That Met QC Criteria
First Posted (Estimate)
Study Record Updates
Last Update Posted (Actual)
Last Update Submitted That Met QC Criteria
Last Verified
More Information
Terms related to this study
Additional Relevant MeSH Terms
Other Study ID Numbers
- cerebellum 1.1
- KLI 252 (Other Grant/Funding Number: Austrian Science Fund)
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