Prosthetic joint infection patterns in critically ill patients who died
Official title: Osteoarticular Sepsis In Intensive Care Units : a Retrospective Study About Deceased Patients.
Run by Assistance Publique - Hôpitaux de Paris · NCT07107685 · Data updated 2026-11-12
This project looks at health records of adults who died in intensive care with a hip, knee, or shoulder prosthetic joint infection from 2018–2022 to see common care paths and outcomes.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years and up |
| Sex | All |
| Enrollment | 150 (estimated) |
| Sponsor | Assistance Publique - Hôpitaux de Paris Academic / other |
| Locations | 1 site (Paris, France) |
| Status | Recruiting |
| Started | September 24, 2025 |
| Main results expected | September 24, 2026 |
| Study ends | September 24, 2026 |
| Registry record updated | June 1, 2026 |
| Trial ID | NCT07107685 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults aged 18 or older who were hospitalized in an intensive care or continuing care unit for at least 48 hours between 2018 and 2022 and died with a primary or associated diagnosis of hip, knee, or shoulder prosthetic joint infection, provided they did not refuse data use.
✕Probably not a fit
Patients with infections of osteosynthesis material or spinal instrumentation, those with multiple infected prostheses, recurrent infections with the same microorganism, persons under legal protection, pregnant or breastfeeding patients, and those deprived of liberty were excluded and therefore will not be represented in the dataset.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This is a retrospective, multicenter review of demographic, clinical, and biological data from adults who died after at least 48 hours in critical care with a prosthetic joint infection between 2018 and 2022. Data from deceased patients will be combined with the OASIS cohort of living critical-care patients with osteoarticular sepsis to broaden comparisons. The analysis will describe patient profiles, care trajectories, microbiology, and outcomes to identify patterns linked to worse prognosis. Results aim to inform identification of at-risk populations and potential improvements in critical-care management of infections involving prosthetic material.
Why it matters
Potential benefit: If successful, the results could help clinicians identify high-risk patients earlier and refine management strategies to reduce complications and deaths from prosthetic joint sepsis.
How similar studies have gone: Previous cohort and registry studies of prosthetic joint infections have identified risk factors and outcomes, and combining deceased-patient data with the OASIS living-patient cohort follows established epidemiologic methods although analysis focused on deceased critical-care patients is less common.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion Criteria: * Patient aged 18 years or older. * Hospitalization in critical care (intensive care unit or continuing care unit) between 2018 and 2022, lasting at least 48 hours, with a prosthetic joint infection (hip, knee, or shoulder prosthesis infection) as the primary or associated diagnosis. * Deceased patient who had not refused data processing. Exclusion Criteria: * Infection involving osteosynthesis material * Infection involving spinal instrumentation * Patient with multiple infected prostheses * Recurrence of prosthetic infection with the same microorganism as a previous episode * Patient under legal protection * Pregnant or breastfeeding patient * Patient deprived of liberty
Where it's running
-
Hôpital Lariboisière
Paris, France, France Recruiting
Study contacts
- Study coordinator: Benjamin SOYER, MD, Msc
- Email: benjamin.soyer@aphp.fr
- Phone: +33 1 49 95 85 15
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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.