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Clinical Trial 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).


Clinical Trial 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. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT06163547
Study type Interventional
Source University Hospital, Geneva
Contact Aria Nouri
Phone +41795530958
Email aria.nouri@hcuge.ch
Status Not yet recruiting
Phase N/A
Start date July 1, 2024
Completion date January 1, 2027

See also
  Status Clinical Trial Phase
Completed NCT02650609 - Treatment of Chronic Subdural Hematoma by Corticosteroids Phase 3
Recruiting NCT04511572 - Embolization of Middle Meningeal Artery in Chronic Subdural Hematoma N/A