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 @ 3:45 AM
Ignite Modification Date:
2025-12-25 @ 3:45 AM
NCT ID:
NCT02941302
Eligibility Criteria:
Inclusion Criteria:
* Histologically confirmed, newly diagnosed intracranial glioma
* A diagnostic contrast enhanced CT/MRI demonstrating the lesion prior to registration
* Patient must sign a study specific informed consent form; if the patient's mental status precludes his/her giving informed consent, written informed consent may be given by the patient's legal representative
Exclusion Criteria:
* Patient without brain gliomas
* Inability to obtain histological proof of glioma (functional domain and particular domain)
* Psychiatric conditions precluding informed consent
* Patients who cannot tolerate operation
* Patients who are pregnant or breast feeding
* Urine pregnancy test will be performed on women of child bearing potential
Healthy Volunteers:
False
Sex:
ALL
Study:
NCT02941302
Study Brief:
Protocol Section:
NCT02941302