Actively Recruiting
Acute Subdural Hematoma Registry
Led by Methodist Health System · Updated on 2026-03-24
100
Participants Needed
1
Research Sites
52 weeks
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are collecting and analyzing data from patients with Acute Subdural Hematoma to better understand the effects of different surgical treatments. This observational study focuses on comparing standard surgical options such as burr hole trephination, craniotomy, decompressive craniectomy, and a newer technique called Middle Meningeal Artery embolization. The goal is to evaluate how these procedures impact survival outcomes in trauma patients. The study gathers information retrospectively from the Methodist Dallas Medical Center Trauma Registry. Data collected includes patient demographics, diagnosis codes, injury details, surgical procedures, complications, laboratory results, and outcomes such as discharge status and mortality. This comprehensive data collection allows researchers to observe real-world treatment effects without altering patient care. Participants are trauma patients aged 18 years or older who have an acute subdural hematoma diagnosed by brain CT or MRI within 72 hours of injury. Researchers will review medical records and imaging to collect relevant information. The primary measurement is the total number of study sites and subjects over five years. There is no active treatment or intervention; instead, the study monitors and analyzes existing clinical data to improve understanding of surgical options and patient outcomes.
CONDITIONS
Brief Title
Acute Subdural Hematoma
Who Can Participate
Eligibility Criteria
You may qualify if you...
- 18 years old or older
- Included in the Methodist Dallas Medical Center Trauma Registry
- Acute subdural hematoma confirmed by brain CT or MRI within 72 hours of trauma
You will not qualify if you...
- Younger than 18 years old
- Prisoners, pregnant persons, or other protected populations
AI-Screening
AI-Powered Screening
Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - Up to 5 years
Participants who undergo routine care are observed through medical record review to collect data on surgical interventions and outcomes related to acute subdural hematoma.
Data collected from routine clinical visits and hospital records
Trial Site Locations
Total: 1 location
1
Methodist Dallas Medical Center- Clinical Research Institute
Dallas, Texas, United States, 75203
Actively Recruiting
Research Team
C
Crystee Cooper, DHEd
K
Kavya Mankulangara
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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