Can a pill tame the inflammation behind brain aneurysms?
NCT ID NCT05959759
First seen Aug 20, 2026 · Last updated Aug 21, 2026 · Updated 1 time
Summary
This trial tests whether dimethyl fumarate, an oral anti-inflammatory medication, can reduce inflammation in the walls of unruptured brain aneurysms. About 60 adults with small, unruptured aneurysms will receive either the drug or a placebo for six months. Using advanced MRI scans, researchers will compare changes in wall inflammation between the two groups to see if the drug has a calming effect.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- dimethyl fumarate, an oral anti-inflammatory drug
- What this could lead to
- If it works, this could point toward a medication-based way to stabilize unruptured brain aneurysms and reduce the need for invasive procedures.
- What could go wrong
- This is a small, early-stage trial. The drug may not reduce inflammation enough to matter, and it can cause side effects like stomach upset or flushing.
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
-
Phase 4
Runs after approval, following long-term safety and how well the treatment works in everyday use.
- Participants
-
60 people
The number who actually took part.
- Started
-
Jul 2023
- Finished
-
Jul 2026
- Lead sponsor
-
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
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Male or female aged ≥18 years. 2. Unruptured IA of ≥3mm identified on imaging (CT, MRI or digital subtraction angiography). 3. Aneurysm wall enhancement identified by HR-VWI before treatment. 4. Ability to understand the objective of the trial with provision of written informed consent. Exclusion Criteria: 1. MRI contraindications (metallic implant, contrast allergy, claustrophobia, etc). 2. Planned treatment of the aneurysm within 6 months. 3. Current treatment with drugs that might have an anti-inflammatory effect (aspirin, statins, immunosuppressive drugs, angiotensin converting enzyme, etc.). 4. Severely impaired liver or renal function. 5. Retreatment of recurrent aneurysm. 6. Pregnant or lactating women. 7. Malignant diseases (liver disease, kidney disease, congestive heart failure, malignant tumours, etc.). 8. Poor compliance with treatment or follow--up (patients who refuse to take medication as prescribed, patients who decline imaging follow--up or blood test, etc).
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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
-
Beijing Neurosurgical Institute & Beijing Tiantan Hospital
Beijing, Beijing Municipality, 100070, China
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