Trials Today

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.	Other: Medical/Phenotype Data Collection Procedures & Data to be Collected TheMethodist Dallas Medical Center Trauma Registry will be queried for demographic information, diagnosis codes, admission dates, traumatic injury characteristics, surgical procedures, comorbidities, inpatient outcomes, complications, consultations, discharge location, and mortality. Additional laboratory values will be abstracted from Epic through retrospective chart review.

Recruiting Locations

Methodist Dallas Medical Center- Clinical Research Institute
Dallas, Texas 75203

Contact:
Colette Ngo Ndjom
214-947-1289
ClinicalResearch@mhd.com

More Details

NCT ID: NCT07490197
Status: Recruiting
Sponsor: Methodist Health System

Study Contact

Crystee Cooper, DHEd
214-947-1280
ClinicalResearch@mhd.com

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.

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.