Analysis of patients with spinal epidural abscess
Prospective Analysis of Spinal Epidural Abscess Associated Outcomes at the University of Kentucky
This study looks at around 200 patients treated for spinal epidural abscesses to see how their medical history and other factors affect their treatment and recovery.
Quick facts
| Study type | Observational |
|---|---|
| Enrollment | 200 (estimated) |
| Ages | 18 Years and up |
| Sex | All |
| Sponsor | University of Kentucky Academic / other |
| Locations | 1 site (Lexington, Kentucky) |
| Trial ID | NCT05464251 on ClinicalTrials.gov |
What this trial studies
This observational study will analyze patients treated for spinal epidural abscess at the University of Kentucky over a two-year period. It aims to enroll approximately 200 patients and will involve a thorough review of clinical, pathological, radiological, and socioeconomic data. The study will begin at the time of patient presentation and continue for one year, focusing on those diagnosed with spinal infections, including those with a history of drug abuse.
Who should consider this trial
Good fit: Ideal candidates include patients diagnosed with spinal epidural abscess, pyogenic vertebral osteomyelitis, or discitis.
Not a fit: Patients who are unwilling or unable to attend follow-up appointments may not benefit from this study.
Why it matters
Potential benefit: If successful, this study could enhance understanding of spinal epidural abscesses and improve treatment strategies for affected patients.
How similar studies have performed: While this study is observational and focuses on a specific condition, similar studies have shown success in understanding spinal infections and their management.
Eligibility criteria
Show full inclusion / exclusion criteria
Inclusion Criteria: * All patient with ICD codes for pyogenic vertebral osteomyelitis, discitis, and spinal epidural abscess will be reviewed for inclusion. Exclusion Criteria: * Patients unwilling or unable to attend follow up appointments.
Where this trial is running
Lexington, Kentucky
- University of Kentucky — Lexington, Kentucky, United States (Recruiting)
Study contacts
- Principal investigator: Francis Farhadi, MD, PhD — University of Kentucky
- Study coordinator: Francis Farhadi, MD, PhD
- Email: francis.farhadi@uky.edu
- Phone: 859-562-0247
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.