Actively Recruiting
Compliance and Tolerance to Oral AntiBiotherapy in Osteoarticular Infections
Led by Hospices Civils de Lyon · Updated on 2025-02-13
60
Participants Needed
1
Research Sites
N/A
Total Duration
On this page
AI-Summary
What this Trial Is About
Researchers are studying bone and joint infections (BJI), which are bacterial infections that can occur after surgery or on their own. Though these infections are rarely fatal in the short term, they can cause significant health problems, reduce quality of life, and increase medical costs. Treatment typically involves antibiotics, often combined with surgery, but the long duration and side effects of antibiotic therapy can make it difficult for patients to stick to their treatment plan. This observational study focuses on patients with BJI who have had surgery and are taking at least one oral antibiotic afterward. The study will measure how well patients adhere to their antibiotic treatment and how well they tolerate it. Adherence will be assessed at 6 weeks and 3 months after surgery using electronic pill dispensers and questionnaires. Tolerance to antibiotics will be evaluated at baseline, 6 weeks, and 3 months post-surgery through patient questionnaires and telephone interviews. Participants will be monitored through questionnaires and electronic devices that track medication use. Data on antibiotic tolerance will be collected at several points, including before and after surgery. Researchers will review the percentage of doses taken at 6 weeks and 3 months as the main outcomes. The study involves telephone follow-ups and data transfers by nursing staff, with total participation lasting at least 3 months after surgery.
CONDITIONS
Brief Title
Compliance and Tolerance to Oral AntiBiotherapy in Osteoarticular Infections (OTABIO)
Who Can Participate
Eligibility Criteria
You may qualify if you...
- Age 18 years or older
- Diagnosed with osteoarticular infection
- Receiving at least one oral antibiotic treatment expected to last 6 weeks or more with a known end date
- Informed about the study and did not object to participate
You will not qualify if you...
- Receiving oral antibiotic treatment for BJI without a known end date
- Receiving only parenteral (intravenous) antibiotic treatment for BJI
- No telephone number or unwilling to provide one
- Adults under legal protection measures
- Pregnant or breastfeeding women
AI-Screening
AI-Powered Screening
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 - 3 months after surgery
Participants are monitored for tolerance and adherence to oral antibiotics prescribed after surgery for osteoarticular infections.
3 visits (baseline, 6 weeks, and 3 months post-surgery) including in-person consultations and telephone interviews
Trial Site Locations
Total: 1 location
1
Hospices Civils de Lyon
Lyon, France, 69004
Actively Recruiting
Research Team
T
Tristan FERRY, MD, PHD
How is the study designed?
Study Type
OBSERVATIONAL
Masking
N/A
Allocation
N/A
Model
N/A
Primary Purpose
N/A
Number of Arms
1
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