Actively Recruiting

Age: 18Years +
All Genders
ID07490197

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

Age: 18Years +
All Genders

Eligibility Criteria

Eligible

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
Not Eligible

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

1
2
3
+1

Your Study Journey

Screening

Duration - 2 to 4 weeks

Participants are screened for eligibility to participate in the trial.

1 visit (in-person)

Surveillance

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

Loading map...

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

Similar Trials

Improving Outcomes for Patients With Critical Bleeding Requi...

Massive Transfusion

Actively Recruiting

1 location

Frequently Asked Questions

Have more questions? Get in touch with our team for quick support

Not the Right Trial for You?

Explore thousands of other clinical trials that might be a better match.
Sign up to get personalized trial recommendations delivered to your inbox.

Already have an account? Log in here