Laser zaps brain tumor regrowth without delaying key therapy
NCT ID NCT07616986
First seen Jun 24, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tests a minimally invasive laser treatment for glioblastoma that regrows shortly after initial surgery, before standard radiotherapy and chemotherapy begin. The goal is to see if the laser can safely treat the regrowth without delaying the planned follow-up treatments. Only 12 adults with glioblastoma will participate, and the main focus is on whether the treatment schedule can be maintained.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Laser interstitial thermal therapy (LITT) - a minimally invasive procedure using heat from a laser to destroy tumor tissue
- What this could lead to
- If successful, this could offer a way to treat early glioblastoma regrowth without delaying standard radiotherapy and chemotherapy, potentially improving survival.
- What could go wrong
- This is a very small, early feasibility study with only 12 participants. The procedure carries risks like bleeding, infection, or brain swelling, and it may not improve outcomes.
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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About 12 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Feb 2026
- Expected to finish
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Jan 2028
An estimate. End dates often move.
- 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 years and older
- 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: * Histologically confirmed glioblastoma, IDH-wildtype, regardless of MGMT status * ≥18 years of age * CRET * Karnofsky Performance Status (KPS) ≥70 * No contra-indication for radio-chemotherapy * Scheduled for adjuvant radio-chemotherapy at University Hospital of Bern * Able to provide informed consent * No contra-indication for LITT * No pregnancy or active breast-feeding * No known coagulopathy independent of medication * No dissemination or multifocal disease * Patients lacking capacity to consent or considered vulnerable (e.g., minors, those under legal protection) are not included. Exclusion Criteria:
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Dep. of Neurosurgery, Bern University Hospital
RECRUITINGBern, 3010, Switzerland
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