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Middle Meningeal Artery Embolization for Chronic Subdural Hematomas (STORMM)

Middle Meningeal Artery (MMA) Embolization for cSDH: Rationale and Design for the STOp Recurrence of MMA Bleeding (STORMM) Randomized-Control Trial

Status
Recruiting
Phases
Unknown
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT06163547
Acronym
STORMM
Enrollment
180
Registered
2023-12-11
Start date
2025-02-18
Completion date
2027-01-01
Last updated
2026-03-17

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Cerebral Compression Due to Injury, Chronic Subdural Hematomas

Brief summary

Chronic Subdural Hematomas (cSHD) are common, and due to cerebral compression, often result in neurological impairment and reduced consciousness. Surgery is typically performed once neurological symptoms develop. Recent studies suggest that arteries nourished by the middle meningeal artery (MMA) may be responsible for hematoma progression and that MMA embolization is clinically useful. There is less evidence, that embolization of MMA also may be a treatment option for individuals without surgical treatment. The investigators propose a multicentre study to investigate both potentials: (1) Assessment of efficacy of embolization after surgery to reduce recurrence and improve outcomes by conducting a randomized trial (randomization arms; Arms 1 and 2), (2) Assessment of embolization-alone efficacy when surgery is contraindicated or refused (embolization-only arm, Arms 3 and 4).

Detailed description

Evidence to support the benefit of MMA embolization remains limited and the risk-benefit balance remains unclear. Case series have shown that recurrence rates with embolization are much lower, and that embolization is generally very safe. Risks associated with neurointerventional procedures will be directly discussed with patients or their caretakers as part of the conventional consenting procedure. Risks include access site hematoma, radiation exposure, vascular injury, brain ischemia, death (theoretic and extremely unlikely) and typical risks associated with general or local anaesthesia. The potential efficacy of MMA embolization as a treatment therefore requires higher level evidence in the form of randomized control trials. The benefit of the embolization is a substantial reduction in recurrence of cSDH, which has been reported to be as high 1 in 3-4 patients. Recurrence of cSDH can lead to additional surgery and complications. First objective: Evaluate the recurrence rates of cSDH after combined surgical and MMA embolization treatments (Arm 2) versus surgery alone (Arms 1). Second objective: The second objective is to evaluate the stability and regression of cSDH after for all the Arms of the study at follow-up.

Interventions

Middle meningeal artery embolization

Sponsors

University Hospital, Geneva
Lead SponsorOTHER

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
NONE

Intervention model description

This study is a multicentre randomised-controlled trial.

Eligibility

Sex/Gender
ALL
Age
18 Years to 100 Years
Healthy volunteers
No

Inclusion criteria

* Age: 18-100 * Consent possible * cSDH located at the convexities * Patients with symptomatic cSDH * Patients with asymptomatic large chronic/subacute hematoma after 6 weeks of failed conservative treatment

Exclusion criteria

* Consent not possible * Pregnancy * Prisoner * Angiography contraindication * Patient for whom follow-up is problematic (e.g. distant residency, homeless …) * Previous surgery for cSDH

Design outcomes

Primary

MeasureTime frameDescription
Recurrence of cSDH - 16-monthsSurgical reoperation
Recurrence of cSDH - 26-monthsNeurological deterioration due to a cSDH after evacuation
Recurrence of cSDH - 36-monthsPost-operative hematoma volume of more than 90% of the preoperative volume at follow-up

Secondary

MeasureTime frameDescription
Additional clinical outcomes - 16-monthsGlasgow Coma Scale (Min=3; Max=15; Higher score=Best outcome)
Additional clinical outcomes - 26-monthsmodified Ranking Scale (Min=0; Max=6; Higher score=Worse outcome)
Additional clinical outcomes - 36-monthsMarkwalder Grading Scale (Min=0; Max=4; Higher score=Worse outcome)
Additional clinical outcomes - 46-monthsGlasgow Outcome Scale - Extended (Min=1; Max=8; Higher score=Best outcome)
Additional clinical outcomes - 56-monthsKarnofsky Performance Score (Min=20; Max=100; Higher score=Best outcome)
Additional clinical outcomes - 66-monthsTherapy-Disability-Neurology grading system (Min=1; Max=5; Higher score=Worse outcome)
Additional clinical outcomes - 76-monthsMortality rate
Additional clinical outcomes - 86-monthsRe-hospitalisation for all causes

Countries

Switzerland

Contacts

CONTACTAria Nouri
aria.nouri@hug.ch+41795530958
PRINCIPAL_INVESTIGATORAria Nouri

University Hospital, Geneva

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Mar 18, 2026