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NCT07091864Recruiting

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

Phase II Randomized Trial Of Glucose Monitoring In Glioblastoma

Source: ClinicalTrials.gov · Last updated 17 Aug 2026

Brief summary (registry, in English)

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 glucose in the blood (hyperglycemia) during radiation therapy is associated with poorer survival outcomes in glioblastoma patients. Hyperglycemia in glioblastoma patients is often driven by steroids that are commonly used during treatment. CGM uses a device that places a sensor under the skin that monitors glucose levels at regular intervals, providing real-time, or near real-time, glucose information. This can help to identify when a patient has changes in their glucose levels so they may receive necessary interventions or medications sooner. CGM may be an effective way for glioblastoma patients to manage their glucose levels, which may improve survival.

Status (registry)
Recruiting
Study type
Interventional
Enrollment
116 (estimated)
First submitted
21 Jul 2025
Start date
29 Jul 2025
Primary completion date
30 Nov 2027
Lead sponsor
Mayo Clinic
Diseases
Glioblastoma
NCT number
NCT07091864

What you commit to

  • Study type: Interventional
  • Planned participants: 116
  • From 29 Jul 2025 to the primary completion date, 30 Nov 2027
  • 3 sites in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Concurrent diagnosis of another active malignancy requiring treatment

Other illness

  • History of eating disorders (e.g., anorexia nervosa, bulimia) or substance use disorder within the past 12 months
  • Any other uncontrolled or inadequately managed medical illness (e.g., unstable cardiovascular, hepatic, renal, or psychiatric condition) that, in the opinion of the investigator, would interfere with study participation or interpretation of results
  • Documented history of type 1 diabetes mellitus

Other

  • Recurrent glioblastoma
  • Pregnancy or breastfeeding at the time of registration

Who the study is looking for

  • 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
  • Negative serum pregnancy test within 7 days prior to registration for individuals of childbearing potential
  • Karnofsky performance status (KPS) ≥ 70 at baseline
  • Absolute neutrophil count (ANC) ≥ 1.5 × 10\^9/L (performed within 14 days prior to registration)
  • Platelet count ≥ 100 × 10\^9/L (performed within 14 days prior to registration)
  • Hemoglobin ≥ 9 g/dL (performed within 14 days prior to registration)
  • Serum creatinine ≤ 1.5 × upper limit of normal (ULN) or creatinine clearance ≥ 60 mL/min (performed within 14 days prior to registration)
  • Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ≤ 2.5 × ULN (performed within 14 days prior to registration)
  • Total bilirubin ≤ 1.5 × ULN (performed within 14 days prior to registration)
  • Willingness and ability to comply with CGM device use and attend dietary counseling sessions as per standard of care

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (3)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Mayo Clinic in Florida
Coordinator of this site? Confirm its status
JacksonvilleUnited StatesNot yet recruiting
Mayo Clinic in Arizona
Coordinator of this site? Confirm its status
PhoenixUnited StatesNot yet recruiting
Mayo Clinic in Rochester
Coordinator of this site? Confirm its status
RochesterUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.