Response Monitoring Trial in Patients With Suspected Recurrence of Glioblastoma
Stopped early · Phase 1
Conditions studied: Glioma, Glioblastoma, Glioblastoma Multiforme
In brief
It was previously shown that \[18F\]Fluorodopa (FDOPA) PET imaging results in intended management changes in 41% of brain tumor patients. However, its impact on patient outcome defined as survival, costs, and/or quality of life has not been demonstrated. Regulatory agencies require randomized trials to determine the impact of PET on patient management and outcome. In this study we hypothesize that the addition of FDOPA PET will improve patient outcome by more accurately identifying presence or absence of tumor recurrence than conventional imaging.
Key facts
- Study ID
- NCT02176720
- Run by
- The Methodist Hospital Research Institute
- People needed
- 31
- Starts
- 2014-05-01
- Expected to finish
- 2016-03-01
- Last updated by the study team
- 2018-08-17
Who can join
Age: 18 and older. Sex: any. Healthy volunteers: not accepted.
You may qualify if…
- Suspected first recurrence of a glioblastoma tumor by clinical measures and/or MRI
- Age 18 and older
You may not qualify if…
- Breast feeding/ Pregnancy
- Severe psychiatric illness
- Primary diagnosis of a glioblastoma
Where it is running
- Houston Methodist Research Institute PET Center — Houston, Texas, United States
Full record on ClinicalTrials.gov
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