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Clinical Trials/NCT04065113
NCT04065113WithdrawnNot Applicable

Middle Meningeal Artery (MMA) Embolization for Patients With Chronic Subdural Hematoma (cSDH)

Washington University School of Medicine1 site in 1 country600 target enrollmentStarted: September 19, 2019Last updated:
Conditions

Trial Snapshot

Phase
Not Applicable
Status
Withdrawn
Enrollment
600
Locations
1
Primary Endpoint
Number of patients with recurrent or refractory hematoma (Radiographic resolution)

Study Overview

Brief Summary

Endovascular middle meningeal artery (MMA) embolization is an emerging treatment for chronic subdural hematoma (cSDH). There is preliminary data to suggest that this minimally invasive therapy may be more efficacious and equally as safe compared to conventional, more invasive surgery. This study seeks to assess the safety and efficacy of middle meningeal artery embolization for chronic subdural hematoma as an adjunct to standard treatments, which include medical management and surgical evacuation.

Detailed Description

This study seeks to assess the safety and efficacy of middle meningeal artery embolization for chronic subdural hematoma in addition to standard treatments, which include close observation and surgical evacuation. Middle meningeal artery embolization has emerged recently as a minimally invasive and successful method of preventing re-accumulation of subdural hematoma, particularly for patients that are not obvious surgical candidates or those with recurrent or refractory hematomas. The outcomes of these two groups of patients who undergo middle meningeal artery embolization will be compared to matched historical controls.

Middle meningeal artery embolization is a minimally invasive angiography procedure completed with use of fluoroscopy. Access is obtained through the femoral or radial artery and a catheter is advanced to the MMA. Polyvinyl alcohol particles are then injected to seal off this portion of the artery and prevent any further blood flow into the subdural hematoma. Hemostasis is obtained at the access site and the patient is observed for 24-48 hours on a neurological care unit before discharge.

A head CT, NIHSS, and modified Rankin Score will be repeated on the following schedule: • Pre-Procedure

  • 24 hours post procedure
  • 7-10 days post procedure
  • 30 days post procedure
  • 90 days post procedure

Patients with chronic subdural hematoma undergo CT scans and neurologic assessments on hospital admission, as well as follow up CT scans and neurologic assessments to assess for any change in neurologic status or hematoma size. This study utilizes a standard of care follow up schedule to avoid exposing participants to extra radiation. Participants will be followed for study related purposes for 90 days.

Study Design

Study Type
Observational
Observational Model
Cohort
Time Perspective
Cross Sectional

Eligibility Criteria

Ages
18 Years to — (Adult, Older Adult)
Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Patients 18 years or older undergoing treatment for a new diagnosis of chronic subdural hematoma (cSDH) or
  • Patients 18 year or older who have undergone surgical evacuation of a subdural hematoma and have a significant residual hematoma status post-surgery or who develop a recurrent subdural hematoma.
  • Minimal symptoms such as headache, altered mental status, or mild neurological deficit only
  • Ability to understand and sign written informed consent by patient or LAR

Exclusion Criteria

  • Significant midline shift and/or neurologic symptoms requiring urgent decompression.
  • Common carotid stenosis of over 50%.
  • Significant contraindication to angiography (eg. kidney failure, difficult anatomy).
  • SDH related to underlying condition
  • Acute SDH

Outcomes

Primary Outcomes

Number of patients with recurrent or refractory hematoma (Radiographic resolution)

Time Frame: A head CT will be repeated 24 hours after the procedure, 7-10 days, 30 days, and 90 days post procedure to measure any change in size of the SDH compared to pre-procedure size

The subdural hematoma persists or reoccurs

Number of patients requiring secondary evacuation surgery (Treatment Efficacy)

Time Frame: Evacuation surgery required within the 90 day follow up period

The participant requires a post-procedure (post-MMA embolization) evacuation of the subdural hematoma due to re-occurrence or persistence of hematoma and symptoms

Secondary Outcomes

  • Procedure-related complication rate (Safety)(Procedure-related complications will be compared between embolization and historical surgical patients assessed through study completion, 90 days)
  • Change in NIH Stroke Scale Score (Functional outcome)(Compared pre-procedure, 24 hours post-procedure, 7-10 days, 30 days, and 90 days post-procedure)
  • Change in modified Rankin Scale (Functional outcome)(Compared pre-procedure, 24 hours post-procedure, 7-10 days, 30 days, and 90 days post-procedure)
  • Change in size of subdural hematoma(Compared pre-procedure, 24 hours post-procedure, 7-10 days, 30 days, and 90 days post-procedure)

Investigators

Sponsor Class
Other
Responsible Party
Sponsor

Study Sites (1)

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