Analysis of patients with spinal epidural abscess
Official title: Prospective Analysis of Spinal Epidural Abscess Associated Outcomes at the University of Kentucky
Run by University of Kentucky · NCT05464251 · Data updated 2026-11-12
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 |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 200 (estimated) |
| Sponsor | University of Kentucky Academic / other |
| Locations | 1 site (Lexington, Kentucky) |
| Status | Recruiting |
| Started | July 12, 2022 |
| Main results expected | June 2027 |
| Study ends | June 2027 |
| Registry record updated | February 13, 2026 |
| Trial ID | NCT05464251 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Ideal candidates include patients diagnosed with spinal epidural abscess, pyogenic vertebral osteomyelitis, or discitis.
✕Probably not a fit
Patients who are unwilling or unable to attend follow-up appointments may not benefit from this study.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
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.
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 gone: While this study is observational and focuses on a specific condition, similar studies have shown success in understanding spinal infections and their management.
Who can join: the full rules
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 it's running
-
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
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.