Could cutting a wider margin around brain tumors extend survival?
NCT ID NCT04737577
First seen Aug 12, 2026 · Last updated Aug 21, 2026 · Updated 3 times
Summary
This pilot trial asks whether removing a wider margin of brain tissue around a high-grade glioma—beyond the standard visible tumor boundary—can improve survival without causing more neurological harm. It enrolls adults with a first-time diagnosis of high-grade glioma in a surgically safe location. Participants are randomly assigned to either standard removal of the enhancing tumor or a supra-marginal resection that extends at least 1 cm into surrounding tissue. The study primarily tests whether a larger trial is feasible, while also tracking survival, neurological function, and quality of life.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Supra-marginal surgical resection (removing a wider margin of brain tissue around the tumor)
- What this could lead to
- If successful, this could show that a wider surgical margin improves survival for people with high-grade glioma, potentially changing standard surgical practice.
- What could go wrong
- This is a small pilot study focused on feasibility, not a definitive test of survival benefit. Removing more brain tissue may increase the risk of neurological problems, and results may not apply to all glioma patients.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Not a phased trial
Phase numbers describe drug development. The registry uses this when they do not apply, as it does for trials of devices, procedures or behaviour changes, and for observational studies.
- Participants
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44 people
The number who actually took part.
- Started
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Feb 2021
- Finished
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Dec 2025
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 85 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Radiographic evidence of a GAD-enhancing intra-axial tumor consistent with HGG; 2. Age ≥18 ≤ 85 years; 3. Karnofsky Performance Score ≥ 60; 4. Location of tumor in a safe anatomical location and 5. Patient or substitute decision maker (SDM) able to understand and consent to study participation. Exclusion Criteria: 1. Multi-focal tumor, gliomatosis cerebri (≥3 lobes of the brain affected), tumors crossing the midline, or leptomeningeal enhancement; 2. Previous craniotomy for tumor excision (stereotactic biopsy is permitted); 3. Known metastatic cancer; 4. Uncorrectable coagulopathy; 5. Unable to obtain GAD-enhanced brain MRI.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Kingston Health Sciences Centre
Kingston, Ontario, K7L 2V7, Canada
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Mackenzie Health Sciences Center
Edmonton, Alberta, T6G 2B7, Canada
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St Michael's Hospital
Toronto, Ontario, M5B 1W8, Canada
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Sunnybrook Health Sciences Centre
Toronto, Ontario, Canada
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The Pennsylvania State University
University Park, Pennsylvania, 16802, United States
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University of Saskatchewan
Saskatoon, Saskatchewan, Canada
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