search
Back to results

Dartmouth Middle Meningeal Embolization Trial (DaMMET) (DAMMET)

Primary Purpose

Chronic Subdural Hematoma, Subdural Hematoma

Status
Recruiting
Phase
Not Applicable
Locations
United States
Study Type
Interventional
Intervention
Embolization of the Middle Meningeal Artery
Standard of care including possible surgical evacuation of subdural hematoma
Sponsored by
Dartmouth-Hitchcock Medical Center
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional treatment trial for Chronic Subdural Hematoma focused on measuring Subdural Hematoma, Chronic Subdural Hematoma, Intracranial Hemorrhage

Eligibility Criteria

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

Inclusion Criteria:

  • 18 years of age or older
  • Have radiographic imaging showing a cSDH > 7mm in maximal thickness encompassing > 50% of the convexity (non-focal).
  • Capable of giving consent for the procedure or have an acceptable surrogate capable of giving consent on the subject's behalf

Exclusion Criteria:

  • The cSDH is secondary to an underlying vascular malformation, tumor, cyst, spontaneous cerebrospinal fluid hypotension or previous craniotomy
  • Life expectancy < 6 months
  • Vascular anatomy that puts the patient at high risk for adverse events (e.g. critical carotid stenosis, abnormal external-internal carotid circulation)
  • Incapable of being reasonably expected to be able to attend follow-up appointments at Dartmouth-Hitchcock Medical Center
  • Vulnerable patients including homeless patients, incarcerated patients and mentally ill patients without appropriate medical decision-making proxy that the physician believes are incapable of appropriately assessing the risks of the procedure

Sites / Locations

  • Dartmouth-Hitchcock Medical CenterRecruiting

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm Type

Active Comparator

Experimental

Active Comparator

Experimental

Arm Label

Symptomatic, standard of care

Symptomatic, MMA embolization + standard of care

Asymptomatic, standard of care

Asymptomatic, standard of care + MMA embolization

Arm Description

Patients in this group will be offered all procedures and care deemed appropriate by the Neurosurgeon in charge of their care. This could include surgical intervention, observation, medical management.

Patients in this group will be treated with the standard of care treatment (the same care described in the arm "Symptomatic, standard of care") but will also undergo MMA embolization of the affected side(s).

Patients in this group will be offered all procedures deemed appropriate by the Neurosurgeon in charge of their care. This could include surgical intervention, observation, medical management.

Patients in this group will be treated with the standard of care treatment (the same care described in the arm "Asymptomatic, standard of care") but will also undergo MMA embolization of the affected side(s).

Outcomes

Primary Outcome Measures

Radiographic resolution of hematoma
CT scan to evaluate for residual hematoma, comparing baseline to 3 months
Radiographic resolution of hematoma
CT scan to evaluate for residual hematoma, comparing baseline to 6 months. Can be canceled if cSDH is completely resolved at 3 months
Radiographic resolution of hematoma
CT scan to evaluate for residual hematoma, comparing baseline to 12 months. Can be canceled if cSDH is completely resolved at 3 or 6 months

Secondary Outcome Measures

Symptomatic improvement
HPI and neurologic exam (standard clinic follow-up) to compare to presenting symptoms.
Symptomatic improvement
HPI and neurologic exam (standard clinic follow-up) to compare to presenting symptoms. This may be canceled if the symptoms and hematoma are completely resolved at 3 months
Symptomatic improvement
HPI and neurologic exam (standard clinic follow-up) to compare to presenting symptoms. This may be canceled if the symptoms and hematoma are completely resolved at 3 or 6 months
NIH Stroke Scale
Comparison of NIHSS at admission to 3 month follow-up
NIH Stroke Scale
Comparison of NIHSS at admission to 6 month follow-up. May be canceled if cSDH resolved by 3 month follow up
NIH Stroke Scale
Comparison of NIHSS at admission to 12 month follow-up. May be canceled if cSDH resolved by 3 or 6 month follow up

Full Information

First Posted
February 8, 2020
Last Updated
February 16, 2023
Sponsor
Dartmouth-Hitchcock Medical Center
search

1. Study Identification

Unique Protocol Identification Number
NCT04270955
Brief Title
Dartmouth Middle Meningeal Embolization Trial (DaMMET)
Acronym
DAMMET
Official Title
A Single Center Randomized Control Trial to Evaluate the Efficacy of Middle Meningeal Artery Embolization in the Treatment of Chronic Subdural Hematomas
Study Type
Interventional

2. Study Status

Record Verification Date
February 2023
Overall Recruitment Status
Recruiting
Study Start Date
March 11, 2020 (Actual)
Primary Completion Date
December 31, 2024 (Anticipated)
Study Completion Date
December 31, 2025 (Anticipated)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Principal Investigator
Name of the Sponsor
Dartmouth-Hitchcock Medical Center

4. Oversight

Studies a U.S. FDA-regulated Drug Product
No
Studies a U.S. FDA-regulated Device Product
No

5. Study Description

Brief Summary
Chronic subdural hematomas (cSDH) are one form of bleeding in the head. They are one of the most common diseases encountered by neurosurgeons across the country. The cSDH can push on the brain and produce symptoms that include seizures, weakness, loss of sensation, and confusion. Many of these cSDH produce repetitive bleeding. Treatment has largely consisted of surgical drainage of hematoma (also known as a blood clot) through either a small hole in the skull or open surgery. However, it is common for the cSDH to reappear despite these procedures. A recent study has shown a treatment failure rate of 27% and a need for additional surgery at 19%. A new approach to treatment of cSDH blocks the blood supply to the tissue that produces the repeated bleeding. Catheters are used to gain access to the middle meningeal artery (MMA), an artery that supplies the coverings of the brain. The artery is blocked using small particles or glue in a process called embolization. A recent pilot study of 72 patients who underwent MMA embolization showed a much lower rate of repeated bleeding. Based on these results, it is thought that this procedure holds promise in reducing the number of cSDH that require one or more operations. The goal of this study is to systematically examine if blocking the blood supply to the tissue responsible for repeated bleeding helps the cSDH resolve and improves patient outcomes.

6. Conditions and Keywords

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

7. Study Design

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

8. Arms, Groups, and Interventions

Arm Title
Symptomatic, standard of care
Arm Type
Active Comparator
Arm Description
Patients in this group will be offered all procedures and care deemed appropriate by the Neurosurgeon in charge of their care. This could include surgical intervention, observation, medical management.
Arm Title
Symptomatic, MMA embolization + standard of care
Arm Type
Experimental
Arm Description
Patients in this group will be treated with the standard of care treatment (the same care described in the arm "Symptomatic, standard of care") but will also undergo MMA embolization of the affected side(s).
Arm Title
Asymptomatic, standard of care
Arm Type
Active Comparator
Arm Description
Patients in this group will be offered all procedures deemed appropriate by the Neurosurgeon in charge of their care. This could include surgical intervention, observation, medical management.
Arm Title
Asymptomatic, standard of care + MMA embolization
Arm Type
Experimental
Arm Description
Patients in this group will be treated with the standard of care treatment (the same care described in the arm "Asymptomatic, standard of care") but will also undergo MMA embolization of the affected side(s).
Intervention Type
Procedure
Intervention Name(s)
Embolization of the Middle Meningeal Artery
Intervention Description
Using established endovascular techniques and materials patient will have a diagnostic catheter based angiogram performed on the side(s) of the brain where the subdural hematoma is present. After verifying the vascular anatomy to ensure safety of the procedure the Middle Meningeal Artery will be embolized.
Intervention Type
Procedure
Intervention Name(s)
Standard of care including possible surgical evacuation of subdural hematoma
Intervention Description
Standard of care could include observation or intervention including surgical drainage of subdural hematoma by bedside drain, Subdural Evacuating Port System (SEPS), burr hole or craniotomy
Primary Outcome Measure Information:
Title
Radiographic resolution of hematoma
Description
CT scan to evaluate for residual hematoma, comparing baseline to 3 months
Time Frame
3 months post-procedure
Title
Radiographic resolution of hematoma
Description
CT scan to evaluate for residual hematoma, comparing baseline to 6 months. Can be canceled if cSDH is completely resolved at 3 months
Time Frame
6 months post-procedure
Title
Radiographic resolution of hematoma
Description
CT scan to evaluate for residual hematoma, comparing baseline to 12 months. Can be canceled if cSDH is completely resolved at 3 or 6 months
Time Frame
12 months post-procedure
Secondary Outcome Measure Information:
Title
Symptomatic improvement
Description
HPI and neurologic exam (standard clinic follow-up) to compare to presenting symptoms.
Time Frame
3 month follow up appointment
Title
Symptomatic improvement
Description
HPI and neurologic exam (standard clinic follow-up) to compare to presenting symptoms. This may be canceled if the symptoms and hematoma are completely resolved at 3 months
Time Frame
6 month follow up appointment
Title
Symptomatic improvement
Description
HPI and neurologic exam (standard clinic follow-up) to compare to presenting symptoms. This may be canceled if the symptoms and hematoma are completely resolved at 3 or 6 months
Time Frame
12 month follow up appointment
Title
NIH Stroke Scale
Description
Comparison of NIHSS at admission to 3 month follow-up
Time Frame
3 months
Title
NIH Stroke Scale
Description
Comparison of NIHSS at admission to 6 month follow-up. May be canceled if cSDH resolved by 3 month follow up
Time Frame
6 months
Title
NIH Stroke Scale
Description
Comparison of NIHSS at admission to 12 month follow-up. May be canceled if cSDH resolved by 3 or 6 month follow up
Time Frame
6 months

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: 18 years of age or older Have radiographic imaging showing a cSDH > 7mm in maximal thickness encompassing > 50% of the convexity (non-focal). Capable of giving consent for the procedure or have an acceptable surrogate capable of giving consent on the subject's behalf Exclusion Criteria: The cSDH is secondary to an underlying vascular malformation, tumor, cyst, spontaneous cerebrospinal fluid hypotension or previous craniotomy Life expectancy < 6 months Vascular anatomy that puts the patient at high risk for adverse events (e.g. critical carotid stenosis, abnormal external-internal carotid circulation) Incapable of being reasonably expected to be able to attend follow-up appointments at Dartmouth-Hitchcock Medical Center Vulnerable patients including homeless patients, incarcerated patients and mentally ill patients without appropriate medical decision-making proxy that the physician believes are incapable of appropriately assessing the risks of the procedure
Central Contact Person:
First Name & Middle Initial & Last Name or Official Title & Degree
Clifford J Eskey, MD/PhD
Phone
6036504477
Email
clifford.j.eskey@hitchcock.org
Facility Information:
Facility Name
Dartmouth-Hitchcock Medical Center
City
Lebanon
State/Province
New Hampshire
ZIP/Postal Code
03756
Country
United States
Individual Site Status
Recruiting
Facility Contact:
First Name & Middle Initial & Last Name & Degree
Clifford J Eskey, MD/PhD
Phone
603-650-4477
Email
clifford.j.eskey@hitchcock.org
First Name & Middle Initial & Last Name & Degree
Daniel R Calnan, MD/PhD
First Name & Middle Initial & Last Name & Degree
Clifford Eskey, MD/PhD
First Name & Middle Initial & Last Name & Degree
Naser Jaleel, MD/PhD
First Name & Middle Initial & Last Name & Degree
Steven Guerin, MD

12. IPD Sharing Statement

Plan to Share IPD
No
IPD Sharing Plan Description
There are no plans to share IPD at this time.

Learn more about this trial

Dartmouth Middle Meningeal Embolization Trial (DaMMET)

We'll reach out to this number within 24 hrs