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NCT07091864 · ClinicalTrials.gov registry record · NA
Continuous Glucose Monitoring for the Management of Hyperglycemia in Patients With Glioblastoma
A NA study of Glioblastoma, IDH-wildtype and WHO Grade 4 Glioma, sponsored by Mayo Clinic.
- Recruiting
- Registry status
- NA
- Development phase
- 116
- Enrollment target
- 1
- Study location
NCT07091864: Recruiting NA study of Glioblastoma, IDH-wildtype and WHO Grade 4 Glioma, sponsored by Mayo Clinic.
NCT07091864 is a NA study of Glioblastoma, IDH-wildtype and WHO Grade 4 Glioma that is actively recruiting participants, run by Mayo Clinic. The registered enrollment target is 116 participants, below the 270-participant average among 15 other Glioblastoma, IDH-wildtype trials with a reported enrollment target (57% lower). The trial reports 1 study location across 1 state. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT07091864, a NA study of Glioblastoma, IDH-wildtype and WHO Grade 4 Glioma, is actively recruiting participants, sponsored by Mayo Clinic.
- RECRUITING
- Registry status
- NA
- Development phase
- 116 participants
- Enrollment target
- 1
- Study location
Study Summary
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.
Primary Outcome
Defined as the time from study enrollment until death due to any cause.
Conditions Studied
Interventions
- PROCEDURE Biospecimen Collection
- PROCEDURE Magnetic Resonance Imaging
- OTHER Best Practice
- OTHER Dietary Intervention
- OTHER Glucose Measurement
Study Locations (1)
Minnesota
- Mayo Clinic in Rochester - Rochester
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 116 participants |
| Start Date | 2025-07-29 |
| Est. Completion | 2027-11-30 |
| Phase | NA |
What NCT07091864 shows while recruiting
NCT07091864 is an interventional study that assigns participants to a tested intervention. The registered 116 participants enrollment target is mid-sized for trials with a published cap, below the 270-participant average among 15 other Glioblastoma, IDH-wildtype trials with a reported enrollment target (57% lower).
The record links to 2 conditions, with Glioblastoma, IDH-wildtype appearing as the primary indexed condition, and to 5 interventions - of which Biospecimen Collection is the first listed.
NCT07091864 reports a single indexed study location in Minnesota.
Frequently Asked Questions
What is clinical trial NCT07091864 about?
NCT07091864 is a clinical study titled "Continuous Glucose Monitoring for the Management of Hyperglycemia in Patients With Glioblastoma". 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 approximate...
What is the current status of trial NCT07091864?
This trial is currently recruiting. It is a NA study. The enrollment target is 116 participants. The study started on 2025-07-29. Estimated completion is 2027-11-30.
What conditions does trial NCT07091864 study?
This clinical trial studies the following conditions: Glioblastoma, IDH-wildtype, WHO Grade 4 Glioma.
What interventions are being tested in trial NCT07091864?
The interventions under investigation include: Biospecimen Collection (PROCEDURE), Magnetic Resonance Imaging (PROCEDURE), Best Practice (OTHER), Dietary Intervention (OTHER), Glucose Measurement (OTHER).
Who is sponsoring clinical trial NCT07091864?
This trial is sponsored by Mayo Clinic, which has 2,844 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT07091864 being conducted?
This trial has 1 study location across Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Glioblastoma, IDH-wildtype
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
Where NCT07091864's enrollment target sits among peer trials
116 8th of 15 higher than 8 of 15 other Glioblastoma, IDH-wildtype trials
participants (enrollment target), bucketed by value
Each bar is a band; taller bars hold more other Glioblastoma, IDH-wildtype trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.
Source ClinicalTrials.gov registry export · 2026-08-08
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