Clinical Trial Details
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NCT02941302 : Multimodality Imaging Combined With Multiple Targets Pathological Examination for Detecting of Biological Borders of Gliomas: a Clinical Application Study
AgesMin: N/A Max: N/A
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

- 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
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