Aneurysm Clinical Trial
Official title:
Cognition and Functional Connectivity After Elective Treatment of Brain Aneurysms
Verified date | January 2018 |
Source | Medical University of Vienna |
Contact | n/a |
Is FDA regulated | No |
Health authority | |
Study type | Observational |
The aim of this proposal is to investigate the effects of uneventful microsurgical and
endovascular treatment of unruptured saccular non-giant anterior communicating artery [ACoA]
aneurysms on resting state functional connectivity levels of higher order cognitive networks
and to correlate the connectivity levels of these networks with neuropsychological
performance and functional outcome.
This study compares two treatment groups and one control group.
Status | Enrolling by invitation |
Enrollment | 57 |
Est. completion date | January 2021 |
Est. primary completion date | July 2019 |
Accepts healthy volunteers | Accepts Healthy Volunteers |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Intervention Groups: Inclusion criteria - Male or female patients aged > 18 years - Microsurgical or endovascular treatment of unruptured, saccular, non giant ACoA aneurysm - Right-handedness - 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) - Willingness and competence to sign informed consent form - German native speaker Exclusion criteria - Ruptured ACoA aneurysm - Previous history of intracranial hemorrhage or serious head injury - Non-saccular aneurysm [i.e. dissecting, fusiform, mycotic, traumatic] - Psychiatric or neuropsychological impairment prior to aneurysm treatment - Current use of any psychotropic drugs except aneurysm treatment related medication - Severe visual or auditory impairment - Current pregnancy or breast feeding - Metallic implants [other than aneurysm clips or coils detailed in the Ethics section] or other contraindications to MRI Healthy controls: Inclusion criteria - Male or female subjects aged > 18 years - Right-handedness - 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] - Willingness and competence to sign informed consent form - German native speaker Exclusion criteria - Major concurrent or previous medical or neurological illness - Major concurrent or previous psychiatric Axis I disorder according to DSM-5 - Clinically significant abnormal values in laboratory screening or general physical examination - Current use of any psychotropic drugs - Previous history of intracranial hemorrhage, serious head injury - Previous or current substance abuse [except nicotine and caffeine] - Severe visual or auditory impairment - Current pregnancy or breast-feeding - Metallic implants or other contraindications to MRI |
Country | Name | City | State |
---|---|---|---|
Austria | Johannes Kepler University Linz, Dept. of Neurosurgery | Linz | Upper Austria |
Austria | Medical University Vienna, Dep. of Neurosurgery | Vienna |
Lead Sponsor | Collaborator |
---|---|
Medical University of Vienna | Johannes Kepler University of Linz |
Austria,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Prefrontal neuronal functional integration measured with fMRI | Changes pre- vs. posttreatment after 2 months | ||
Secondary | Prefrontal executive functioning measured with neuropsychological tests | Changes pre- vs. posttreatment after 2 months (short-term outcome) and after 12 months (long-term outcome). | ||
Secondary | Correlation of changes on neuropsychological (executive functioning) and neuronal level (fMRI). | Changes pre- vs. posttreatment after 2 months measured with fMRI correlated with changes in neuropsychological tests after 2 months (short-term outcome) and after 12 months (long-term outcome). |
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