G81.9 C71.0
Conditions
Interventions
Sponsors
Eligibility
Inclusion criteria
Inclusion criteria: 1.) Patients with status post supratentorial brain tumor resection with a new occurred or progressive paresis postoperatively 2.) Written consent of the patient for participating in the study 3.) older or equal than 18 years
Exclusion criteria
Exclusion criteria: 1.) Patients with contraindication for MRI-imaging 2.) Patients with contraindication for TMS examination (e.g. metallic implants) 3.) More than one generalized seizure per week 4.) Pregnancy 5.) Disagreement of the patient for participating in the study 6.) younger than 18 years
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Fugl Meyer assessment of the upper extremity after 3 months, assessed by an experienced blinded physiotherapist. | — |
Secondary
| Measure | Time frame |
|---|---|
| Fugl Meyer Assessment of the upper extremity postoperatively, on day of discharge and after 1 month, assessed by an experienced blinded physiotherapist. Nine Hole Peg Test (NHPT), Finger Tapping Test, Karnofsky Performance Status Scale (KPS), muscle strength (BMRC) postoperatively, on day of discharge, after 1 and 3 months, assessed by an experienced blinded physiotherapist. National Institutes of Health Stroke Scale (NIHSS), Karnofsky Performance Status Scale (KPS) postoperatively, on day of discharge, after 1 and 3 months, assessed by a blinded physician. Quality of life (EORTC questionnaire) postoperatively, on day of discharge, after 1 and 3 months. Duration between tumor resection and receiving adjuvant therapy | — |
Countries
Germany
Contacts
Klinik für Neurochirurgie Charité - Universitätsmedizin Berlin