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Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
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Register:
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ClinicalTrials.gov |
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Last refreshed on:
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5 July 2021 |
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Main ID: |
NCT04938362 |
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Date of registration:
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13/06/2021 |
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Prospective Registration:
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No |
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Primary sponsor: |
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Public title:
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Cognitive Function and Fatigue After Brain Abscess
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Scientific title:
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Cognitive Function and Fatigue After Brain Abscess |
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Date of first enrolment:
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January 1, 2020 |
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Target sample size:
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50 |
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Recruitment status: |
Recruiting |
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URL:
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https://clinicaltrials.gov/show/NCT04938362 |
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Study type:
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Observational |
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Study design:
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Phase:
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Countries of recruitment
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Norway
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Contacts
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Name:
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Bjørnar Hassel, MD, PhD |
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Address:
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Telephone:
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+4722118080 |
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Email:
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bjornar.hassel@medisin.uio.no |
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Affiliation:
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Name:
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Peder H Utne |
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Address:
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Telephone:
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+4723066023 |
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Email:
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pedutn@ous-hf.no |
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Affiliation:
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Name:
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Daniel Dahlberg, MD, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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Oslo University Hospital |
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Name:
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Bjørnar Hassel, MD, PhD |
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Address:
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Telephone:
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Email:
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Affiliation:
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University of Oslo |
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Key inclusion & exclusion criteria
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Inclusion criteria:
• Patients who have completed treatment for brain abscess and who agree to participate.
Exclusion criteria:
- Patients who cannot undergo neuropsychological investigation due to unconsciousness
- Patients who cannot undergo neuropsychological investigation, being mentally too ill
- Patients who suffer from dementia
- Patients who cannot undergo FDG-PET due to claustrophobia
- Age under 16.
Age minimum:
16 Years
Age maximum:
N/A
Gender:
All
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Health Condition(s) or Problem(s) studied
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Brain Abscess
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Cognitive Dysfunction
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Fatigue
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Intervention(s)
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Other: FDG-PET
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Primary Outcome(s)
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A change in FDG-PET signal indicating a change in neuronal activity
[Time Frame: When all patients have been followed up for at least 1 year.]
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A change in FDG-PET signal indicating inflammation
[Time Frame: When all patients have been followed up for at least 1 year.]
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Secondary Outcome(s)
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Fatigue after brain abscess
[Time Frame: When all patients have been followed up for at least 1 year.]
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No fatigue after brain abscess
[Time Frame: When all patients have been followed up for at least 1 year.]
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Secondary ID(s)
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Cognition/fatigue/brainabscess
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Source(s) of Monetary Support
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Please refer to primary and secondary sponsors
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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