Chronic Subdural Hematoma Clinical Trial
Official title:
Pilot Study to Evaluate Safety of and Efficacy of Middle Meningeal Artery (MMA) Embolization Compared to Traditional Surgical Strategies to Treat Chronic Subdural Hematomas (cSDH)
Chronic Subdural Hematoma (cSDH) is a common hematologic problem particularly in older patients. The purpose of this study is to evaluate the safety and efficacy of middle meningeal artery (MMA) embolization compared to traditional surgical strategies for patients presenting with chronic subdural hematoma (cSDH). Although MMA embolization is minimally-invasive procedure that is routinely used for the treatment of tumors or vascular formations (1), this study investigates the use of an established procedure for a new disease state.
Status | Recruiting |
Enrollment | 50 |
Est. completion date | April 19, 2022 |
Est. primary completion date | April 19, 2022 |
Accepts healthy volunteers | No |
Gender | All |
Age group | 18 Years and older |
Eligibility |
Inclusion Criteria: - Age 18 or older - Participant or Surrogate must be English speaking - Subjects must have a diagnosis of chronic or acute-on subdural hematoma based on brain imaging, as documented by an - One or more symptoms attributable to chronic SDH including headache cognitive impairment, gait instability, seizure, or mild focal neurologic deficit. - In opinion of Investigator or the subject's referring physician, the subject has failed conservative management. Exclusion Criteria: - The Subdural hematoma is causing mass effect significant enough to cause marked or progressive neurologic impairment - Any requirement for urgent surgical evacuation is necessary - Life expectancy is less than 6 months in the opinion of the subject's primary physician - Markedly tortuous vasculature precluding safe endovascular access, as assessed on angiogram - Acute subdural hematomas - Health insurance doesn't cover MMA embolization or performing Surgeon and follow up visits are considered out of network. - Pregnancy |
Country | Name | City | State |
---|---|---|---|
United States | Overlook Medical Center | Summit | New Jersey |
Lead Sponsor | Collaborator |
---|---|
Atlantic Health System |
United States,
Type | Measure | Description | Time frame | Safety issue |
---|---|---|---|---|
Primary | Change in size of SDH | Changes in size of SDH will be recorded in maximum diameter within 6 months. | 6 months | |
Secondary | Change in Neurological status | Changes in Neurological status after the procedure and through study completion | 6 months |
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