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Search / Trial NCT01089244

FET-PET for Diagnosis and Monitoring in Patients With Low Grade Glioma

Launched by LUDWIG-MAXIMILIANS - UNIVERSITY OF MUNICH · Mar 17, 2010

Trial Information

Current as of June 06, 2025

Unknown status

Keywords

Low Grade Glioma Astrocytoma Molecular Imaging Fet Pet Therapy Monitoring Temodar

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • neuroradiologically suspected low grade glioma (Astrocytoma WHOI-II, Oligodendroglioma WHO II, Oligoastrocytoma WHO II)
  • histological verification will be obtained either by microsurgery or by stereotactic biopsy
  • patients older than 18 years
  • Karnofsky Performance Score \>=70
  • pregnant or nursing female patients will not be included in this study
  • Exclusion Criteria:
  • patients in whom informed consent cannot be obtained due to organic brain syndrome or insufficient language skills
  • patients who cannot lie quiet for a time period of app. two hours during the FET-PEt scan
  • medical history of a metastatic brain disease
  • patients in whom an MRI scan cannot be performed due to claustrophobia metallic protheses or pacemakers etc.

About Ludwig Maximilians University Of Munich

Ludwig-Maximilians-University of Munich (LMU Munich) is a prestigious research institution in Germany, renowned for its commitment to advancing medical science and improving patient care through innovative clinical research. As a leading sponsor of clinical trials, LMU Munich leverages its extensive academic resources and interdisciplinary expertise to conduct rigorous studies aimed at evaluating new therapeutic interventions and advancing healthcare knowledge. The university fosters collaboration among researchers, clinicians, and healthcare professionals, ensuring that trials are designed and executed with the highest ethical standards and scientific integrity. Through its dedication to excellence in research, LMU Munich aims to contribute significantly to the development of effective treatments and enhance the overall health outcomes for diverse patient populations.

Locations

Munich, Bavaria, Germany

Duesseldorf, North Rhine Westphalia, Germany

Patients applied

0 patients applied

Trial Officials

Joerg C. Tonn, Prof. Dr.

Principal Investigator

Department of Neurosurgery, LMU Munich

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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