Continuous Glucose Monitoring for the Management of Hyperglycemia in Patients With Glioblastoma

Recruiting N/A Interventional Study
Glioblastoma, IDH-Wildtype WHO Grade 4 Glioma
No Placebo Group Every participant receives an active treatment — no one gets a placebo.
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At a Glance
Age
18 and older
Sex
Any
Study type
Interventional
Purpose
Supportive Care
Participants needed
116 (estimated)
Sponsor
Mayo Clinic · Other
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About This Trial
This clinical trial studies whether continuous glucose monitoring (CGM) can be used to help patients with glioblastoma manage their blood sugar (glucose) levels and improve survival. Glioblastoma is the most common malignant primary brain tumor in adults, with an average survival time of approximately 15-18 months despite therapy. Studies have shown that having a higher-than-normal amount of gluco…
Trial Locations
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Eligibility Criteria
Inclusion Criteria: * Presumed newly diagnosed GBM based on imaging findings consistent with GBM on brain MRI (e.g., heterogeneously enhancing mass with central necrosis and surrounding edema), as determined by the treating neuro-oncology team * Age ≥ 18 years at the time of consent * Karnofsky per…
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Clinical Trials Referral Office

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mayocliniccancerstudies@mayo.edu

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