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Middle Meningeal Artery Embolization for Chronic Subdural Hematoma

Primary Purpose

Chronic Subdural Hematoma

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Middle Meningeal Artery Embolization with polyvinyl alcohol particles (PVA)
Drainage of Subdural Hematoma
Sponsored by
Washington University School of Medicine
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Subdural Hematoma

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

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.

and

  • 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

Sites / Locations

  • Washington University School of MedicineRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Experimental

Experimental

No Intervention

Active Comparator

Arm Label

Embolization Only

Embolization + Evacuation

Medical Management

Surgical Patients

Arm Description

Medically managed patient receives middle meningeal artery embolization

Participant receives standard of care evacuation and then undergoes MMA embolization

Historical control of medically managed patients

Historical control of patients receiving standard surgery alone

Outcomes

Primary Outcome Measures

Number of patients with recurrent or refractory hematoma (Radiographic resolution)
The subdural hematoma persists or reoccurs
Number of patients requiring secondary evacuation surgery (Treatment Efficacy)
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 Outcome Measures

Procedure-related complication rate (Safety)
Complication rate of embolization procedure vs surgery
Change in NIH Stroke Scale Score (Functional outcome)
Change in score on National Institutes of Health Stroke Scale. The NIH Stroke Scale is used to quantify neurologic impairments. It consists of 11 items each scored between 0 and 4 points. The maximum score is 42, indicating severe impairment, and the minimum score is 0. Stroke severity 0 No stroke symptoms 1-4 Minor stroke 5-15 Moderate stroke 16-20 Moderate to severe stroke 21-42 Severe stroke
Change in modified Rankin Scale (Functional outcome)
Change in score on modified Rankin Scale The modified Rankin Scale (mRS) measures the degree of disability or dependence after a stroke or other neurologic disease. The scale runs from 0-6, with 0 indicating perfect health with no symptoms to 6 indicating death. 0 - No symptoms. - No significant disability. Able to carry out all usual activities, despite some symptoms. - Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities. - Moderate disability. Requires some help, but able to walk unassisted. - Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted. - Severe disability. Requires constant nursing care and attention, bedridden, incontinent. - Dead.
Change in size of subdural hematoma
CT scan measurements of size of subdural hematoma

Full Information

First Posted
August 15, 2019
Last Updated
May 19, 2022
Sponsor
Washington University School of Medicine
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1. Study Identification

Unique Protocol Identification Number
NCT04065113
Brief Title
Middle Meningeal Artery Embolization for Chronic Subdural Hematoma
Official Title
Middle Meningeal Artery (MMA) Embolization for Patients With Chronic Subdural Hematoma (cSDH)
Study Type
Interventional

2. Study Status

Record Verification Date
May 2022
Overall Recruitment Status
Recruiting
Study Start Date
September 19, 2019 (Actual)
Primary Completion Date
August 18, 2024 (Anticipated)
Study Completion Date
January 1, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Washington University School of Medicine

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
Yes
Product Manufactured in and Exported from the U.S.
No
Data Monitoring Committee
No

5. Study Description

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.

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Subdural Hematoma

7. Study Design

Primary Purpose
Treatment
Study Phase
Not Applicable
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
600 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
Embolization Only
Arm Type
Experimental
Arm Description
Medically managed patient receives middle meningeal artery embolization
Arm Title
Embolization + Evacuation
Arm Type
Experimental
Arm Description
Participant receives standard of care evacuation and then undergoes MMA embolization
Arm Title
Medical Management
Arm Type
No Intervention
Arm Description
Historical control of medically managed patients
Arm Title
Surgical Patients
Arm Type
Active Comparator
Arm Description
Historical control of patients receiving standard surgery alone
Intervention Type
Procedure
Intervention Name(s)
Middle Meningeal Artery Embolization with polyvinyl alcohol particles (PVA)
Other Intervention Name(s)
MMA Embolization with polyvinyl alcohol (PVA) particles
Intervention Description
Seal off blood supply to the middle meningeal artery to prevent growth of subdural hematoma
Intervention Type
Procedure
Intervention Name(s)
Drainage of Subdural Hematoma
Other Intervention Name(s)
Burr Hole Drainage, Craniotomy
Intervention Description
Drainage of subdural hematoma via burrhole or craniotomy
Primary Outcome Measure Information:
Title
Number of patients with recurrent or refractory hematoma (Radiographic resolution)
Description
The subdural hematoma persists or reoccurs
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
Title
Number of patients requiring secondary evacuation surgery (Treatment Efficacy)
Description
The participant requires a post-procedure (post-MMA embolization) evacuation of the subdural hematoma due to re-occurrence or persistence of hematoma and symptoms
Time Frame
Evacuation surgery required within the 90 day follow up period
Secondary Outcome Measure Information:
Title
Procedure-related complication rate (Safety)
Description
Complication rate of embolization procedure vs surgery
Time Frame
Procedure-related complications will be compared between embolization and historical surgical patients assessed through study completion, 90 days
Title
Change in NIH Stroke Scale Score (Functional outcome)
Description
Change in score on National Institutes of Health Stroke Scale. The NIH Stroke Scale is used to quantify neurologic impairments. It consists of 11 items each scored between 0 and 4 points. The maximum score is 42, indicating severe impairment, and the minimum score is 0. Stroke severity 0 No stroke symptoms 1-4 Minor stroke 5-15 Moderate stroke 16-20 Moderate to severe stroke 21-42 Severe stroke
Time Frame
Compared pre-procedure, 24 hours post-procedure, 7-10 days, 30 days, and 90 days post-procedure
Title
Change in modified Rankin Scale (Functional outcome)
Description
Change in score on modified Rankin Scale The modified Rankin Scale (mRS) measures the degree of disability or dependence after a stroke or other neurologic disease. The scale runs from 0-6, with 0 indicating perfect health with no symptoms to 6 indicating death. 0 - No symptoms. - No significant disability. Able to carry out all usual activities, despite some symptoms. - Slight disability. Able to look after own affairs without assistance, but unable to carry out all previous activities. - Moderate disability. Requires some help, but able to walk unassisted. - Moderately severe disability. Unable to attend to own bodily needs without assistance, and unable to walk unassisted. - Severe disability. Requires constant nursing care and attention, bedridden, incontinent. - Dead.
Time Frame
Compared pre-procedure, 24 hours post-procedure, 7-10 days, 30 days, and 90 days post-procedure
Title
Change in size of subdural hematoma
Description
CT scan measurements of size of subdural hematoma
Time Frame
Compared pre-procedure, 24 hours post-procedure, 7-10 days, 30 days, and 90 days post-procedure

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
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. and 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
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Joshua W Osbun, MD
Organizational Affiliation
Washington University School of Medicine
Official's Role
Principal Investigator
Facility Information:
Facility Name
Washington University School of Medicine
City
Saint Louis
State/Province
Missouri
ZIP/Postal Code
63108
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Brigette Vaughn, BA
Phone
314-273-0368
Email
b.vaughn@wustl.edu
First Name & Middle Initial & Last Name & Degree
Joshua W Osbun, MD

12. IPD Sharing Statement

Plan to Share IPD
Yes

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Middle Meningeal Artery Embolization for Chronic Subdural Hematoma

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