Acute Subdural Hematoma
Purpose
This retrospective data repository will serve as a means to aggregate and analyze standard surgical interventions and Middle Meningeal Arteryembolization as suitable treatment options for Acute Subdural Hematoma.
Condition
- Trauma
Eligibility
- Eligible Ages
- Over 18 Years
- Eligible Sex
- All
- Accepts Healthy Volunteers
- No
Inclusion Criteria
- ≥18 years old - Included in the Methodist Dallas Medical Center Trauma Registry - Acute subdural hematoma identified on computed tomography scan or magnetic resonance imaging of the brain in the trauma bay within 72 hours of a traumatic event
Exclusion Criteria
- <18 years old - Prisoners, pregnant persons, or other protected population
Study Design
- Phase
- Study Type
- Observational
- Observational Model
- Other
- Time Perspective
- Retrospective
Arm Groups
| Arm | Description | Assigned Intervention |
|---|---|---|
| Total Number and Description of Study Sites/Total Number of Subjects | This study will include all trauma patients who meet registry inclusion and arrive at the Methodist Dallas Medical Center trauma bay with Acute subdural hematoma . Enrollment will terminate once adequate number of interventions have been observed for clinical significance to be established. |
|
Recruiting Locations
Methodist Dallas Medical Center- Clinical Research Institute
Dallas, Texas 75203
Dallas, Texas 75203
More Details
- NCT ID
- NCT07490197
- Status
- Recruiting
- Sponsor
- Methodist Health System
Detailed Description
The primary objective of this study is to establish a data repository permissive of quality improvement studies/observations specific to patients with Acute Subdural Hematoma and evaluate impact of surgical interventions like burr hole trephination, Craniotomy, Decompressive Craniectomy, and Middle Meningeal Arteryembolization embolization on survival outcomes.