Glioblastoma Clinical Trial
Official title:
Use of TTFields in Germany in Routine Clinical Care Study PROgram - Daily Activity, Sleep and Neurocognitive Functioning in Newly Diagnosed Glioblastoma Patients Study
This non-interventional study aims to investigate change over time in cognitive function, sleep quality, and activity in daily life as important determinants of QoL in a large cohort of GBM patients in Germany treated with TTFields in routine clinical care using low-threshold, electronic PRO and modern automated tracking data analyses. The gained results will allow even better understanding of TTFields therapy in daily life of GBM patients and consequently, better informing patients about what to expect when starting this therapy, increasing therapy compliance in the long-term.
Status | Recruiting |
Enrollment | 500 |
Est. completion date | February 1, 2025 |
Est. primary completion date | December 1, 2024 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility | Inclusion Criteria: - min.18 years of age - Newly diagnosed, histologically confirmed GBM - Patient after completion of radiochemotherapy but within first 3 cycles of first-line tumor-specific maintenance chemotherapy - Clinical indication of treatment with NovoTTF-200A System (Optune®) according to IFU and medical guidelines - Signed informed consent Exclusion Criteria: Any foreseeable deviation from the IFU of NovoTTF-200T Device |
Country | Name | City | State |
---|---|---|---|
Germany | Universitätsklinikum Aachen | Aachen | |
Germany | Klinikum Aschaffenburg-Alzenau | Aschaffenburg | |
Germany | Universitätsklinikum Augsburg (AöR) | Augsburg | |
Germany | Universitätsklinikum Bonn | Bonn | |
Germany | Klinikum Chemnitz | Chemnitz | |
Germany | Carl-Thiem-Klinikum Cottbus | Cottbus | |
Germany | Universitätsklinik Carl Gustav Carus Dresden | Dresden | |
Germany | Sana Kliniken Duisburg | Duisburg | |
Germany | Universitätsklinikum Düsseldorf HHU | Düsseldorf | |
Germany | HELIOS Klinikum Erfurt | Erfurt | |
Germany | Universitätsklinikum Erlangen | Erlangen | |
Germany | Universitätsklinikum Essen | Essen | |
Germany | Universitätsklinikum Frankfurt Goethe-Universität | Frankfurt | |
Germany | Universitätsmedizin Greifswald | Greifswald | |
Germany | BG Klinikum Bergmannstrost Halle | Halle | |
Germany | Medizinische Hochschule Hannover | Hannover | |
Germany | Onkologische Schwerpunktpraxis Dres. I. Zander und E. von der Heyde | Hannover | |
Germany | Universitätsklinikum des Saarlandes | Homburg | |
Germany | Universitätsklinikum Jena | Jena | |
Germany | Klinikum Kassel | Kassel | |
Germany | Universitätsklinikum SH Campus Kiel | Kiel | |
Germany | Kliniken der Stadt Köln GmbH | Köln | |
Germany | Uniklinik Köln | Köln | |
Germany | Otto-von-Guericke-Universität Magdeburg | Magdeburg | |
Germany | Med. Fakultät Mannheim der Universität Heidelberg | Mannheim | |
Germany | Johannes Wesling Klinikum Minden | Minden | |
Germany | Kliniken Maria Hilf GmbH | Mönchengladbach | |
Germany | Klinikum Nürnberg | Nürnberg | |
Germany | Pius-Hospital Oldenburg | Oldenburg | |
Germany | Niels-Stensen-Kliniken - Marienhospital Osnabrück | Osnabrück | |
Germany | Universitätsmedizin Rostock | Rostock | |
Germany | HELIOS Kliniken Schwerin GmbH | Schwerin | |
Germany | Johanniter-Krankenhaus Genthin-Stendal GmbH | Stendal | |
Germany | Klinikum Stuttgart | Stuttgart | |
Germany | Universitätsklinikum Tübingen | Tübingen | |
Germany | Paracelsus-Klinik Zwickau | Zwickau |
Lead Sponsor | Collaborator |
---|---|
NovoCure Ltd. |
Germany,
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* Note: There are 22 references in all — Click here to view all references
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Time of usage of TTFields treatment in follow-up derived from monitoring data of the devices, standardised to usage days, as measure of compliance with TTFields treatment. | Time of usage (compliance) of TTFields treatment over time is measured using the treatment compliance report at the Follow-up period | through study completion, an average of 18 months (mean follow-up time) | |
Primary | Number of TTFields treatment-related SAEs as assessed by the CEC standardized to one year of FU time | Number of TTFields treatment-related SAEs standardized to one year of follow-up (FU) is measured using the collection of SAEs during the follow-up period | through study completion, an average of 18 months (mean follow-up time) | |
Primary | Changes in daily physical activity as a potential quality of life parameter in TTFields treatment compared to baseline for up to four months after start of TTFields therapy | Changes in daily physical activity will be assessed by smartphone app-based clinical monitoring. | Up to 4 months after start of TTFields treatment compared to baseline | |
Primary | Changes in sleep quality as a potential quality of life parameter in TTFields treatment compared to baseline for up to four months after start of TTFields therapy | Changes in sleep quality will be assessed by smartphone app-based clinical monitoring. | Up to 4 months after start of TTFields treatment compared to baseline | |
Primary | Changes in neurocognitive functioning as a potential quality of life parameter in TTFields treatment compared to baseline for up to four months after start of TTFields therapy. | Changes in neurocognitive functioning will be assessed by means of MoCA interview tests. | Up to 4 months after start of TTFields treatment compared to baseline |
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