Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 2:54 AM
Ignite Modification Date:
2025-12-25 @ 2:54 AM
NCT ID:
NCT03531333
Eligibility Criteria:
Inclusion Criteria:
* Individuals of 18 years or older
* Newly diagnosed, untreated, contrast enhancing presumed high-grade glioma
* KPS ≥ 60
* Preoperative intention to perform gross-total resection of the enhancing tumor
* Written informed consent conform ICH-GCP
Exclusion Criteria:
* Tumours crossing the midline basal ganglia, cerebellum, or brain stem prohibiting gross total resection
* Multifocal contrast enhancing lesions
* Pre-existing neurological deficit (e.g. aphasia, hemiparesis) due to neurological diseases (e.g. stroke)
* Inability to give consent because of dysphasia or language barrier
Healthy Volunteers:
False
Sex:
ALL
Minimum Age:
18 Years
Study:
NCT03531333
Study Brief:
Protocol Section:
NCT03531333