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NCT07757113Not yet recruiting

Comparative Study of Embolic Agents in Patients With Subdural Hemorrhage Undergoing Middle Meningeal Artery (MMA) Embolization

Source: ClinicalTrials.gov · Last updated 11 Aug 2026

Brief summary (registry, in English)

Single site, prospective, comparative effectiveness pilot trial comparing efficacy and safety outcomes of three embolic materials (particles, liquid embolics, and Wallaby Phenox coils) in MMA embolication for cSDH.

Status (registry)
Not yet recruiting
Study type
Interventional
Enrollment
30 (estimated)
First submitted
31 Jul 2026
Start date
1 Sept 2026
Primary completion date
30 Sept 2027
Lead sponsor
Sanford Health
Diseases
Stroke
NCT number
NCT07757113

What you commit to

  • Study type: Interventional
  • Planned participants: 30
  • From 1 Sept 2026 to the primary completion date, 30 Sept 2027
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Other illness

  • Known severe allergy or contraindication to embolic materials (e.g. particles, liquids like Onyx/n-BCA, or coils)
  • Inability to undergo angiography (e.g. severe renal impairment contraindicating contrast)

Other

  • Ineligible for MMAE procedure, as deemed by the treating physician, for any indication (e.g. pregnancy)
  • Non-chronic subdural hematoma (cSDH) indications for Middle Meningeal Artery Embolization (MMAE), including acute subdural hematoma with symptom onset \< 72 hours or mixed acute/chronic without predominant chronic features
  • Pregnancy or breastfeeding
  • Inability or unwillingness to complete follow-up visits at 30 and 90 days

Who the study is looking for

  • Adult patients (≥ 18 years)
  • Undergoing Middle Meningeal Artery Embolization (MMAE) for chronic subdural hematoma (cSDH)
  • Able to provide informed consent or have a legally authorized representative (LAR) do so

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Sanford USD Medical Center
Coordinator of this site? Confirm its status
Sioux FallsUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.