Actively Recruiting
Economic-demographic Assessment of the Aseptic Mobilization of Knee Prostheses Through the RIPO Registry and Radiographic Analysis of the Case Series From the II Clinic of IOR
Led by Istituto Ortopedico Rizzoli · Updated on 2026-04-21
31
Participants Needed
1
Research Sites
N/A
Total Duration
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AI-Summary
What this Trial Is About
Researchers are studying the issue of aseptic mobilization, which is the loosening of knee prostheses without infection, in patients who have undergone total knee arthroplasty (TKA). This condition often leads to revisions of the knee replacement and places a significant burden on healthcare resources. The study aims to analyze the causes of aseptic mobilization and its economic impact within the Emilia Romagna region of Italy. This observational study involves evaluating demographic data, healthcare expenses, and radiographic images over a 24-month period. The researchers will use the RIPO Registry and radiographic analysis of cases from the II Clinic of Istituto Ortopedico Rizzoli to assess the problem and identify areas for improvement. Participants will be patients who have undergone knee prosthesis revision due to aseptic mobilization and have at least two years of follow-up. The study will monitor demographic information, analyze healthcare costs related to the condition, and perform radiographic assessments during the 24 months. The involvement includes collecting data and reviewing images to better understand the condition and its impact.
CONDITIONS
Brief Title
Economic-demographic Assessment of the Aseptic Mobilization of Knee Prostheses Through the RIPO Registry and Radiographic Analysis of the Case Series From the II Clinic of IOR
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Patients undergoing knee prosthesis revision for aseptic mobilization
- Follow-up of at least 2 years
- Willingness to participate in the study
- Both sexes
- Patients 18 years old or older
You will not qualify if you...
- Patient refusal to participate in the study and sign the informed consent
- Simultaneous participation in other studies
AI-Screening
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Complete this quick 3-step screening to check your eligibility
Your Study Journey
Duration - 2 to 4 weeks
Participants are screened for eligibility to participate in the trial.
1 visit (in-person)
Duration - 24 months
Participants who have undergone knee prosthesis revision for aseptic mobilization are observed over time to collect demographic data, healthcare expenses, and radiographic analysis results.
Follow-up visits as part of routine clinical care over 24 months
Trial Site Locations
Total: 1 location
1
IRCCS Istituto Ortopedico Rizzoli
Bologna, Bologna, Italy, 40136
Actively Recruiting
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
0
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