Spinal infection study aims to measure Real-World recovery rates
NCT ID NCT07509983
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This observational study will follow 50 patients with primary spondylodiscitis, a serious spinal infection, for one year. Researchers will track cure rates, pain levels, and daily function using standard treatments like antibiotics and braces. The goal is to understand how well current care works in a real hospital setting.
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Study facts
What this study's own registry entry says, in plain language.
- Participants
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About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
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May 2026
An estimate. Start dates often move.
- Expected to finish
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Jun 2029
An estimate. End dates often move.
- Lead sponsor
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Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
The study population comprises patients of any age or sex presenting to the Orthopedic and Trauma Surgery Department (encompassing both inpatient wards and outpatient clinics) at Assiut University Hospital with clinical symptoms and/or radiological findings suggestive of primary pyogenic (bacterial) spondylodiscitis.
- Ages
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Children (under 18), adults (18 to 64) and older adults (65 and over)
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * All patients presenting to Assiut University Hospital and its affiliated outpatient clinics with clinical symptoms and/or radiological findings suggestive of primary pyogenic (bacterial) spondylodiscitis, regardless of age or sex. Exclusion Criteria: * Patients with postoperative or iatrogenic spinal infections (secondary spondylodiscitis following spinal surgery or instrumentation). * Non-pyogenic spondylodiscitis. * Patients with incomplete medical records or insufficient follow-up data. * Patients who decline to provide informed consent.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The official record
The full official record for this study. This one lists no contact details, but it is the first place any would appear.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
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Other studies related to the condition(s) this trial covers.