Registry of adults with head and neck trauma at Methodist Dallas Medical Center
Head and Neck Trauma Registry, Protocol ID: 032.MBSI.2021.D
This study collects information from adults who have had head and neck injuries at Methodist Dallas Medical Center to see how they were treated and what their outcomes were.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 30 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | Methodist Health System Academic / other |
| Locations | 1 site (Dallas, Texas) |
| Trial ID | NCT05592899 on ClinicalTrials.gov |
What this trial studies
This observational study collects retrospective data on adults who have experienced cervical and/or skull base fractures or subdural hematomas at Methodist Dallas Medical Center since January 2016. The registry aims to gather a statistically significant number of cases to analyze outcomes and treatment patterns. Data will be sourced from electronic health records without any additional tests or procedures for participants. The study does not involve direct patient contact, ensuring that treatment decisions remain unaffected.
Who should consider this trial
Good fit: Ideal candidates are adults aged 18 and older who have presented with cervical and/or skull base fractures or subdural hematomas at the medical center.
Not a fit: Patients who do not meet the inclusion criteria or belong to vulnerable populations may not benefit from this study.
Why it matters
Potential benefit: If successful, this registry could enhance understanding of head and neck trauma outcomes, potentially leading to improved treatment protocols.
How similar studies have performed: While this approach is observational and retrospective, similar registries have successfully contributed to understanding trauma outcomes in other settings.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patients 18 years of age or older * Presenting to MDMC with cervical and/or skull base fractures or those with subdural hematomas Exclusion Criteria: * Do not meet the Study Inclusion Criteria laid out in section 4.1. * Vulnerable populations
Where this trial is running
Dallas, Texas
- Methodist Moody Brain and Spine Institute, Methodist Dallas Medical Center — Dallas, Texas, United States (Recruiting)
Study contacts
- Principal investigator: Michael Oh, MD, PhD — Methodist
- Study coordinator: Crystee Cooper, DHEd
- Email: clinicalresearch@mhd.com
- Phone: 214-947-1280
How to participate
- Review the eligibility criteria above with your treating physician.
- Visit the official trial page on ClinicalTrials.gov for the most current contact information and recruitment status.
- Contact the listed study coordinator or principal investigator to request pre-screening. Pre-screening is free and never obligates you to enroll.