Menu
Recruiting NCT07490197

Acute Subdural Hematoma

Observational Trauma

For patients and families

In plain language

An automatic summary of structured registry data. It is an orientation aid, not a substitute for the official protocol or a physician assessment.

What is being studied
The protocol lists: Medical/Phenotype Data Collection Procedures & Data to be Collected.
Who it may be relevant to
Registry conditions: Trauma. Basic parameters: from 18 years · All.
What needs checking
Age, condition and sex are only basic indicators. Prior treatment, laboratory values and other mandatory requirements appear in the eligibility criteria below.
Where it takes place
United States
Next step
Save the trial, show it to the treating physician, and confirm current recruitment with the study center. Costs, documents and travel →
Official title

Acute Subdural Hematoma Registry

Overview

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.

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.

Interventions

  • 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.

Primary outcome measures

  • Total Number of Study Sites [Time frame: 5 years]

Eligibility criteria

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

Criteria are shown verbatim from the registry (in English). Final eligibility is always assessed by the study center.

Study design

Observational model
Other

Study locations

United States · 1 center
  • Methodist Dallas Medical Center- Clinical Research Institute — Dallas

Identifiers

NCT: NCT07490197 · 060.TRA.2023.D

Primary sources (government registries)

View this study on ClinicalTrials.gov ↗